NDC Product
Human Otc DrugMenthol Cough Drops Creamy Strawberry Flavor NDC 10202-012
- Generic Name
- Menthol And Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Malic Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 817L1N4CKP.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 6915-15-7 and the RxNorm Concept ID (RxCUI) 29209. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
MALIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
817L1N4CKP
The specific atomic composition represented as a molecular structure string.
InChIKey
C4H6O5 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
BJEPYKJPYRNKOW-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(C(=O)O)C(C(=O)O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Malic Acid. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
MALIC ACID
OF
Common Names & Synonyms
(+/-)-MALIC ACID
CN
D,L-MALIC ACID
CN
DL-MALIC ACID
CN
HYDROXYBUTANEDIOIC ACID [HSDB]
CN
HYDROXYSUCCINIC ACID
CN
MALATE
CN
MALIC ACID (CONSTITUENT OF CRANBERRY LIQUID PREPARATION) [DSC]
CN
MALIC ACID [EP MONOGRAPH]
CN
MALIC ACID [FCC]
CN
MALIC ACID [II]
CN
MALIC ACID [MI]
CN
MALIC ACID [NF]
CN
MALIC ACID [USP IMPURITY]
CN
MALIC ACID [USP-RS]
CN
MALIC ACID [VANDF]
CN
MALIC ACID [WHO-DD]
CN
MALIC ACID, DL-
CN
POMALOUS ACID
CN
Systematic Nomenclature
2-HYDROXYBUTANEDIOIC ACID
SYS
HYDROXYBUTANEDIOIC ACID, (+/-)-
SYS
Technical Codes
E296
CD
E-296
CD
INS NO. 296
CD
INS NO.296
CD
INS-296
CD
NSC-25941
CD
NDC Products Containing MALIC ACID
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (375), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
7-ELEVEN
Active Listing
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugLevocarnitine NDC 70954-139
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevocarnitine NDC 70954-140
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
ATLANTIC BIOLOGICALS CORP.
NDC Product
Human Prescription DrugAripiprazole NDC 17856-0684
- Generic Name
- Aripiprazole Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Affordable Pharmaceuticals, LLC
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 10572-012
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 10572-112
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals LLC
NDC Product
Human Prescription DrugSodium Oxybate NDC 65162-065
- Generic Name
- Sodium Oxybate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 65162-649
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEscitalopram Oxalate NDC 65162-705
- Generic Name
- Escitalopram
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 65162-893
- Generic Name
- Aripiprazole
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals NY LLC
NDC Product
Human Prescription DrugEnalapril Maleate NDC 69238-1729
- Generic Name
- Enalapril
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 69238-2027
- Generic Name
- Spironolactone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVancomycin Hydrochloride NDC 69238-2261
- Generic Name
- Vancomycin Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Apotex Corp.
NDC Product
Human Prescription DrugAripiprazole NDC 60505-0404
- Generic Name
- Aripiprazole
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Army & Air Force Exchange Service
NDC Product
Human Otc DrugExchange Select Drops Sugar Free Lemon Mint NDC 55301-586
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ascend Laboratories, LLC
NDC Product
Human Prescription DrugOxcarbazepine NDC 67877-532
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 67877-725
- Generic Name
- Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugEscitalopram Oxalate NDC 65862-248
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Azurity Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSuprep Bowel Prep NDC 24338-175
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSuprep Bowel Prep NDC 24338-177
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSuflave NDC 24338-550
- Generic Name
- Polyethylene Glycol 3350, Sodium Sulfate, Potassium Chloride...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Bionpharma Inc.,
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate, And Magnesium Sulfate NDC 69452-428
- Generic Name
- Sodium Sulfate, Potassium Sulfate, And Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Braintree Laboratories, Inc.
NDC Product
Human Prescription DrugSuprep Bowel Prep NDC 52268-012
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSuflave NDC 52268-550
- Generic Name
- Polyethylene Glycol 3350, Sodium Sulfate, Potassium Chloride...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 63629-1130
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 63629-1131
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 63629-1132
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 63629-1133
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 71335-2724
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 72162-1652
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 72162-1653
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 72162-1654
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 72162-2088
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
CP Skin Health Group, Inc.
NDC Product
Human Otc DrugEltamd Uv Active NDC 72043-2600
- Generic Name
- Zinc Oxide, Titanium Dioxide Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 31722-098
- Generic Name
- Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEscitalopram Oxalate NDC 31722-569
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-684
- Generic Name
- Aripiprazole Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 31722-691
- Generic Name
- Spironolactone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSodium Oxybate NDC 31722-891
- Generic Name
- Sodium Oxybate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 110, LLC. DBA Leader
NDC Product
Human Otc DrugLeader Throat Soothing Drops Creamy Strawberry NDC 70000-0711
- Generic Name
- Throat Soothing Creamy Strawberry
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugAripiprazole NDC 62135-904
- Generic Name
- Aripiprazole
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugZicam Cold Remedy Zinc And Elderberry Lozenge NDC 10237-462
- Generic Name
- Zinc Acetate Anhydrous, Zinc Gluconate, And Sambucus Nigra F...
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Acetate Anhydrous And Zinc Gluconate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy Medicated Fruit Drops - Assorted Fruit NDC 10237-468
- Generic Name
- Zinc Acetate Anhydrous And Zinc Gluconate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy Medicated Fruit Drops - Elderberry NDC 10237-469
- Generic Name
- Zinc Acetate Anhydrous, Zinc Gluconate, And Sambucus Nigra F...
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy NDC 10237-473
- Generic Name
- Zinc Acetate Anhydrous And Zinc Gluconate
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Cosmetic Enterprise Ltd
NDC Product
Human Otc DrugIlluminating Spf 50 Plus Drops Broad Spectrum Sunscreen NDC 56152-0253
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories
NDC Product
Human Otc DrugBlue Lizard Sheer Spf 50 Sunscreen NDC 0316-2059
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Derma Care Research Labs
NDC Product
Human Otc DrugDch Rapid Relief Hemorrhoidal NDC 72839-263
- Generic Name
- Lidocaine 5%, Phenylephrine Hydrochloride 0.25%
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Dermalogica, LLC.
NDC Product
Human Otc DrugGolden Hour Hydrating Spf 30 NDC 68479-420
- Generic Name
- Octocrylene, Octisalate, And Avobenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Deseret Biologicals
NDC Product
Human Otc DrugEnergize NDC 43742-2047
- Generic Name
- Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosu...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Deseret Biologicals, Inc.
NDC Product
Human Otc DrugDetox I NDC 43742-1488
- Generic Name
- Carduus Marianus, Chelidonium Majus, Lycopodium Clavatum, Ta...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCirculation NDC 43742-1510
- Generic Name
- Cactus Grandiflorus, Kali Carbonicum, Kalmia Latifolia, Arni...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugEnergize NDC 43742-1568
- Generic Name
- Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosu...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugBact Combination NDC 43742-2239
- Generic Name
- Adenosinum Triphosphoricum Dinatrum, Cinnamic Acid, Colibaci...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugBio Co Enzyme Phase NDC 43742-2259
- Generic Name
- Aconiticum Acidum, Cis-, Adenosinum Triphosphoricum Dinatrum...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Dr. Donna Restivo DC
NDC Product
Human Otc DrugD1 Organ Support NDC 62185-0052
- Generic Name
- Carduus Marianus, Chelidonium Majus, Lycopodium Clavatum, Ta...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Energique, Inc.
NDC Product
Human Otc DrugSpleenex Vh NDC 44911-0294
- Generic Name
- Aralia Quinquefolia, Ginkgo Biloba, Pancreas Suis, Spleen (s...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugLiverex I NDC 44911-0419
- Generic Name
- Ginkgo Biloba, Fel Tauri, Gallbladder (suis), Hepar Suis), T...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugLungex Ii NDC 44911-0439
- Generic Name
- Ginkgo Biloba, Colon (suis), Lung (suis), Pancreas Suis, Ger...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugSpleenex V NDC 44911-0539
- Generic Name
- Aralia Quinquefolia, Potassium Gluconate, Ginkgo Biloba, Mag...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugKidnex Iv NDC 44911-0747
- Generic Name
- Ginkgo Biloba, Alpha-ketoglutaricum Acidum, Citricum Acidum,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMitochondria Pro NDC 44911-0903
- Generic Name
- Aralia Quinquefolia, Arnica Montana, Adenosinum Triphosphori...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Exeltis USA, Inc.
NDC Product
Human Prescription DrugSelect-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0075
- Generic Name
- .beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Expanscience Laboratories d/b/a Mustela
NDC Product
Human Otc DrugMustela Mineral Sunscreen Broad Spectrum Spf 50 NDC 64768-2924
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Farmacy Beauty LLC
NDC Product
Human Otc DrugGreen Defense Broad Spectrum Spf 30 NDC 72830-261
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ferring Pharmaceuticals Inc.
NDC Product
Human Prescription DrugClenpiq NDC 55566-6800
- Generic Name
- Sodium Picosulfate, Magnesium Oxide, And Anhydrous Citric Ac...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- NDA
Active Listing
Guna spa
NDC Product
Human Otc DrugOmeosport NDC 17089-075
- Generic Name
- .alpha.-ketoglutaric Acid - Aconitic Acid, Cis - Adenosine T...
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-lympho NDC 17089-291
- Generic Name
- Apis Mellifera - Calendula Officinalis Flower - Centella Asi...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-dizzy NDC 17089-306
- Generic Name
- .alpha.-ketoglutaric Acid - Ambergris - Anamirta Cocculus Se...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-geriatrics NDC 17089-349
- Generic Name
- 1,4-benzoquinone - Arnica Montana - Oxytocin - Barium Carbon...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-matrix NDC 17089-416
- Generic Name
- Ascorbic Acid - Dodecahydroxycyclohexane Dihydrate - Fucus V...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMicox NDC 17089-420
- Generic Name
- Aspergillus Niger Var. Niger - Candida Albicans - Centella A...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna Matrix Detox NDC 17089-460
- Generic Name
- Sodium Sulfate - Podophyllum Peltatum Root - Solidago Virgau...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna Lympho Detox NDC 17089-462
- Generic Name
- Aesculus Hippocastanum - Apis Mellifera - Calendula Officina...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
HY-VEE, INC
NDC Product
Human Otc DrugHyvee Throat Drops Lemon Mint NDC 42507-907
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugCitrucel NDC 0135-0090
- Generic Name
- Methylcellulose
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPreparation H Rapid Relief NDC 0573-2890
- Generic Name
- Lidocaine, Phenylephrine Hydrochloride
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
June Jacobs Labs LLC
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Paste
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
June Jacobs Labs, LLC
NDC Product
Human Otc DrugAnti-aging Blemish Control Peel Pads NDC 65278-318
- Generic Name
- Salicylic Acid
- Dosage Form
- Swab
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Paste
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kao USA Inc.
NDC Product
Human Otc DrugHello Sunday The Shimmer One Mineral Glow Spf 45 NDC 10596-805
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kobayashi Healthcare International, Inc.
NDC Product
Human Otc DrugNauzene Chewables Ginger Honey NDC 52389-677
- Generic Name
- Sodium Citrate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Leadiant Biosciences, Inc.
NDC Product
Human Prescription DrugCarnitor NDC 54482-145
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCarnitor Sf NDC 54482-148
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate, Magnesium Sulfate NDC 43386-700
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
MODULAR THERMAL TECHNOLOGIES LLC DBA LIFE WEAR TECHNOLOGIES
NDC Product
Human Otc DrugTricalm Hydrogel NDC 71207-221
- Generic Name
- Aluminum Acetate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugEscitalopram NDC 33342-053
- Generic Name
- Escitalopram
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Method Pharmaceuticals, LLC
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 58657-160
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 58657-161
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Fluoride Chewable NDC 58657-162
- Generic Name
- Sodium Fluoride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Modular Thermal Technologies LLC Dba Life Wear Technologies
NDC Product
Human Otc DrugTricalm Hydrogel NDC 71207-100
- Generic Name
- Aluminum Acetate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
Mondelez Global LLC
NDC Product
Human Otc DrugHalls Green Apple NDC 12546-118
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHalls Blueberry NDC 12546-119
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBreezers Cool Berry NDC 12546-151
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBreezers Creamy Strawberry NDC 12546-352
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHalls Breezers Sugar Free Cool Berry NDC 12546-720
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.
NDC Product
Human Otc DrugGelato Homecare NDC 68400-201
- Generic Name
- Stannous Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGelato Homecare NDC 68400-205
- Generic Name
- Stannous Fluoride
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NSE Products, Inc.
NDC Product
Human Otc DrugNutricentials Here You Glow Exfoliating Toner NDC 62839-1339
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 72603-278
- Generic Name
- Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 72603-445
- Generic Name
- Aripiprazole Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novel Laboratories, Inc.
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate, Magnesium Sulfate NDC 40032-700
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Precision Dose, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 68094-123
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Prestige Brands Holdings, Inc.
NDC Product
Human Otc DrugLudens Watermelon Throat Drops NDC 52183-102
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Watermelon Throat Drops NDC 52183-202
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Green Apple Throat Drops NDC 52183-204
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Strawberry Banana Throat Drops NDC 52183-209
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Assorted Flavors NDC 52183-217
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Wild Cherry Throat Drops NDC 52183-229
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Sugar Free Wild Cherry Throat NDC 52183-249
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Berry Assortment Throat Drops NDC 52183-289
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLudens Wild Cherry Throat Drops NDC 52183-299
- Generic Name
- Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pro Weight Loss Inc.
NDC Product
Human Otc DrugThyro Support NDC 70558-0009
- Generic Name
- Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosu...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Professional Complementary Health Formulas
NDC Product
Human Otc DrugArsenicum Combination 9251 NDC 63083-9251
- Generic Name
- Arsenicum Combination
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugThyroid Nosode Combination 9420 NDC 63083-9420
- Generic Name
- Thyroid Nosode Combination
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
QUAGEN PHARMACEUTICALS LLC
NDC Product
Human Prescription DrugAripiprazole NDC 70752-114
- Generic Name
- Aripiprazole
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
RB Health (US) LLC
NDC Product
Human Otc DrugMucinex Childrens Mighty Chews Cough NDC 72854-081
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ricola Ag
NDC Product
Human Otc DrugDual Action Cherry Cough Suppressant Oral Anesthetic NDC 54305-313
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDual Action Cherry Cough Suppressant Oral Anesthetic NDC 54305-331
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 54305-507
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 54305-517
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCherry Throat Drops NDC 54305-518
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 54305-909
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCherry Throat Drops NDC 54305-910
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ricola USA Inc.
NDC Product
Human Otc DrugDual Action Cherry Cough Suppressant Oral Anesthetic NDC 63667-224
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDual Action Cherry Cough Suppressant Oral Anesthetic NDC 63667-242
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 63667-507
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 63667-517
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCherry Throat Drops NDC 63667-518
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCherry Throat Drops NDC 63667-952
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatural Cherry Honey Herb Throat Drops NDC 63667-953
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugEscitalopram Oxalate NDC 16571-769
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevocarnitine NDC 64980-503
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
SPF Ventures LLC
NDC Product
Human Otc DrugBrush On Block Quick Stick Spf 40 Mineral Stick NDC 58274-012
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Saptalis Pharmaceuticals, LLC
NDC Product
Human Prescription DrugLevocarnitine NDC 71656-016
- Generic Name
- Levocarnitine Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sato Pharmaceutical Co., Ltd.
NDC Product
Human Otc DrugSatohap NDC 49873-018
- Generic Name
- Dl-camphor, L-menthol, Methyl Salicylate
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSatogesic NDC 49873-060
- Generic Name
- Dl-camphor, L-menthol, Methyl Salicylate
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSatogesic Hot NDC 49873-608
- Generic Name
- Capsaicin
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSatohap Cool And Hot Pads NDC 49873-621
- Generic Name
- Camphor, Capsaicin, Menthol
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sato Pharmaceuticals Co., Ltd.
NDC Product
Human Otc DrugSatohap Cool And Hot NDC 49873-622
- Generic Name
- Camphor, Capsaicin, Menthol
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Schwabe North America, Inc
NDC Product
Human Otc DrugCold Flu Relief Berry NDC 53499-0349
- Generic Name
- Cold Flu Relief Berry
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Relief Kids Cherry NDC 53499-3351
- Generic Name
- Pelargonium Sidoides
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Relief Kids Cherry NDC 53499-5522
- Generic Name
- Pelargonium Sidoides
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Relief Cherry NDC 53499-6144
- Generic Name
- Pelargonium Sidoides
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Schwabe North America, Inc.
NDC Product
Human Otc DrugCold Flu Relief Orange NDC 53499-0161
- Generic Name
- Cold Flu Relief Orange
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Flu Relief Berry Chewable NDC 53499-1159
- Generic Name
- Pelargonium Sidoides, Aconitum Napellus, Bryonia, Eucalyptus...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Relief Kids Fastactives Cherry NDC 53499-2166
- Generic Name
- Pelargonium Sidoides
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugSambucus Cold Flu Relief Elderberry NDC 53499-5175
- Generic Name
- Pelargonium Sidoides Root, Aconitum Napellus, Eucalyptus Glo...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Schwabe North American, Inc.
NDC Product
Human Otc DrugAllergy And Sinus Relief NDC 53499-4194
- Generic Name
- Pelargonium Sidoides Root, Hydrastis Canadensis Whole, Potas...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Solventum US LLC
NDC Product
Human Otc Drug3m Skin And Nasal Antiseptic NDC 17518-060
- Generic Name
- Povidone-iodine
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Strides Pharma Science Limited
NDC Product
Human Prescription Drug- Generic Name
- Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate Oral
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugEscitalopram NDC 51672-1348
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Sodium Sulfate Anhydrous, Potassium Sulfate, And Magnesium S...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
TRUPHARMA, LLC
NDC Product
Human Prescription DrugLevocarnitine NDC 52817-830
- Generic Name
- Levocarnitine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Podiatree Company
NDC Product
Human Otc DrugVeraciti NDC 54633-115
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugKlor-con NDC 0245-0360
- Generic Name
- Potassium Chloride
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
VistaPharm, LLC
NDC Product
Human Prescription DrugAripiprazole NDC 66689-735
- Generic Name
- Aripiprazole
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugChildrens Daytime Mucus NDC 0363-9358
- Generic Name
- Dextromethorphan Hbr
- Dosage Form
- Chewable Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Nighttime Mucus NDC 0363-9360
- Generic Name
- Dextromethorphan Hbr Doxylamine Succinate
- Dosage Form
- Chewable Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDaytime Nighttime Chewable NDC 0363-9393
- Generic Name
- Dextromethorphan Hbr Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Co
NDC Product
Human Otc DrugWalgreens Pain Relief With Lidocaine NDC 0363-1026
- Generic Name
- Lidocaine, Phenylephrine Hcl
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wilshire Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 52536-175
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSodium Sulfate, Potassium Sulfate And Magnesium Sulfate NDC 52536-177
- Generic Name
- Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- NDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugZituvio NDC 70771-1770
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvio NDC 70771-1771
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvio NDC 70771-1772
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70771-1790
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70771-1791
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70771-1792
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugZituvimet NDC 70771-1859
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet NDC 70771-1860
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1869
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1870
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1879
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1880
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1881
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1886
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1887
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1888
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Zydus Pharmaceuticals (USA) Inc.
NDC Product
Human Prescription DrugZituvio NDC 70710-1240
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvio NDC 70710-1241
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvio NDC 70710-1242
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet NDC 70710-1786
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet NDC 70710-1787
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70710-1899
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70710-1900
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin NDC 70710-1901
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-1986
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-1987
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1804
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1805
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1806
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2036
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2037
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2038
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
doTERRA International, LLC
NDC Product
Human Otc DrugDoterra Sun NDC 71630-173
- Generic Name
- Zinc Oxide
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDoterra Sun NDC 71630-175
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
