NDC Product
Human Prescription DrugLupron Depot NDC 0074-3346
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Stearic Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 4ELV7Z65AP.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 57-11-4 and the RxNorm Concept ID (RxCUI) 1310551. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
STEARIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
4ELV7Z65AP
The specific atomic composition represented as a molecular structure string.
InChIKey
C18H36O2 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
QIQXTHQIDYTFRH-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
CCCCCCCCCCCCCCCCCC(=O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Stearic 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
STEARIC ACID
OF
Common Names & Synonyms
ADEKA SA 300
CN
BAROLUB FTA
CN
CENTURY 1210
CN
DERVACID 3155
CN
HYDROFOL ACID 150
CN
N-OCTADECANOIC ACID
CN
PURIFIED STEARIC ACID
CN
PURIFIED STEARIC ACID [NF]
CN
STEARATE
CN
STEARIC ACID (CONSTITUENT OF EVENING PRIMROSE OIL) [DSC]
CN
STEARIC ACID (CONSTITUENT OF FLAX SEED OIL) [DSC]
CN
STEARIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]
CN
STEARIC ACID [DSC]
CN
STEARIC ACID [EP MONOGRAPH]
CN
STEARIC ACID [FHFI]
CN
STEARIC ACID [HSDB]
CN
STEARIC ACID [II]
CN
STEARIC ACID [JAN]
CN
STEARIC ACID [MART.]
CN
STEARIC ACID [MI]
CN
STEARIC ACID [USP-RS]
CN
STEARIC ACID [VANDF]
CN
STEARIC ACID [WHO-DD]
CN
Systematic Nomenclature
OCTADECANOIC ACID
SYS
Technical Codes
FEMA NO. 3035
CD
NSC-25956
CD
NSC-261168
CD
NDC Products Containing STEARIC 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 (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
AbbVie Inc.
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3473
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3642
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3683
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugDiclofenac Sodium NDC 0228-2550
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Sodium NDC 0228-2551
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPilocarpine Hydrochloride NDC 0228-2801
- Generic Name
- Pilocarpine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugPilocarpine Hydrochloride NDC 0228-2837
- Generic Name
- Pilocarpine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Allergan, Inc.
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugLamotrigine NDC 0115-1526
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-1527
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-1528
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-1529
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1800
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1801
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1802
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPyridostigmine Bromide NDC 0115-2134
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPyridostigmine Bromide NDC 0115-3511
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-9939
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-9940
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-9941
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0115-9942
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
BF ASCHER AND CO INC
NDC Product
Human Otc DrugMobisyl NDC 0225-0360
- Generic Name
- Trolamine Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bausch Health US, LLC
NDC Product
Human Prescription DrugMestinon NDC 0187-3010
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMestinon NDC 0187-3013
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5160
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5162
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5164
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5170
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5172
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoritate NDC 0187-5202
- Generic Name
- Metronidazole
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugMidol Bloat Relief NDC 0280-0070
- Generic Name
- Pamabrom
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAleve Back And Muscle Pain NDC 0280-0111
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Headache Pain NDC 0280-0112
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve NDC 0280-0113
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Caplets NDC 0280-0114
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Easy Open Arthritis NDC 0280-0131
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Plus Cold And Flu Fizzychews NDC 0280-0151
- Generic Name
- Chlorpheniramine Maleate, Acetaminophen, Dextromethorphan Hy...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Plus Cough And Sore Throat Fizzychews NDC 0280-0152
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Plus Day Severe Cold Plus Flu NDC 0280-0921
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, A...
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAleve Gelcaps NDC 0280-6020
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAleve Gelcaps NDC 0280-6070
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMidol Long Lasting Relief NDC 0280-8090
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAleve Headache Pain NDC 0280-8252
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugFleet NDC 0132-0075
- Generic Name
- Glycerin
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFleet NDC 0132-0401
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPedia-lax NDC 0132-0655
- Generic Name
- Magnesium Hydroxide
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories
NDC Product
Human Otc DrugPanoxyl NDC 0316-0227
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanoxyl NDC 0316-0228
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSarna NDC 0316-0230
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlue Lizard Sensitive Sunscreen NDC 0316-2045
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlue Lizard Kids Spf 50 Sunscreen NDC 0316-2062
- Generic Name
- Octisalate And Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories, Inc
NDC Product
Human Otc DrugSarna NDC 0316-0234
- Generic Name
- Pramoxine Hydrochloride, Menthol
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0201
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0202
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0203
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0277
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
E.R. Squibb & Sons, L.L.C.
NDC Product
Human Prescription DrugEvotaz NDC 0003-3641
- Generic Name
- Atazanavir And Cobicistat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugPenicillamine NDC 0254-2000
- Generic Name
- Penicillamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitisinone NDC 0254-3020
- Generic Name
- Nitisinone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitisinone NDC 0254-3021
- Generic Name
- Nitisinone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitisinone NDC 0254-3022
- Generic Name
- Nitisinone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Galderma Laboratories, L.P.
NDC Product
Human Otc DrugCetaphil Sheer Mineral Sunscreen Stick Spf 50 NDC 0299-4108
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Daily Facial Moisturizer With Suncreen Spf 35 NDC 0299-4113
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Acne Relief Body Wash NDC 0299-4121
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Sheer Mineral Sunscreen Spf 50 NDC 0299-4122
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDifferin Acne Clearing Body Wash NDC 0299-4131
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Healthy Renew Day Cream Broad Spectrum Spf 30 NDC 0299-4136
- Generic Name
- Homosalate, Octocrylene, Octisalate, Avobenzone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Hydrating Face Sunscreen Spf 35 NDC 0299-4142
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Gentle Clear Pore Clearing Acne Cleanser NDC 0299-4143
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Daily Facial Moisturizer With Suncreen Spf 50 NDC 0299-4930
- Generic Name
- Octinoxate, Octisalate, Octocrylene, Oxybenzone, Titanium Di...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugTri-luma NDC 0299-5950
- Generic Name
- Fluocinolone Acetonide, Hydroquinone, And Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugRobitussin Direct Sore Throat Pain NDC 0031-9301
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-2001
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Headache NDC 0067-2002
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Headache NDC 0067-2003
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-2039
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-2040
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Relief NDC 0067-2042
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Pm Triple Action Caplets NDC 0067-2056
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Diphenhydramine Citrate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8136
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8137
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Tension Headache NDC 0067-8139
- Generic Name
- Acetaminophen, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Regular Strength Stimulant Laxative NDC 0067-8141
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Caplets NDC 0067-8145
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength And Excedrin Tension Headache NDC 0067-8151
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr And Acetaminophen, Chlor...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-8201
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-8202
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-8203
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon Extra Strength NDC 0135-0098
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon Extra Strength NDC 0135-0430
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFlonase Headache And Allergy Relief NDC 0135-0578
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Nondrowsy NDC 0135-0607
- Generic Name
- Acetaminophen And Phenyleprine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Pm NDC 0135-0608
- Generic Name
- Acetaminophen And Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Extra Strength NDC 0135-0609
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Extra NDC 0135-0620
- Generic Name
- Acetaminophen And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Extra Strength NDC 0135-7011
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Pm NDC 0135-7021
- Generic Name
- Acetaminophen And Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Nondrowsy NDC 0135-7031
- Generic Name
- Acetaminophen And Phenyleprine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Day NDC 0135-7033
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Night NDC 0135-7034
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugPyrazinamide NDC 0054-0812
- Generic Name
- Pyrazinamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugPrednisone NDC 0054-0017
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0018
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0019
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0235
- Generic Name
- Morphine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0236
- Generic Name
- Morphine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0243
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0244
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0245
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAminocaproic Acid NDC 0054-1100
- Generic Name
- Aminocaproic Acid
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAminocaproic Acid NDC 0054-1110
- Generic Name
- Aminocaproic Acid
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-3294
- Generic Name
- Furosemide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-3298
- Generic Name
- Furosemide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone Intensol NDC 0054-3721
- Generic Name
- Prednisone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-3722
- Generic Name
- Prednisone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4297
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4299
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4301
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiskets NDC 0054-4538
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMercaptopurine NDC 0054-4581
- Generic Name
- Mercaptopurine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4728
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4741
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4742
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8297
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8299
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8301
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8724
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8739
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8740
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9817
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9818
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9828
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 0143-1171
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 0143-1172
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 0143-1173
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCaptopril NDC 0143-1174
- Generic Name
- Captopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
L Perrigo Company
NDC Product
Human Otc DrugGood Sense Dual Action NDC 0113-5300
- Generic Name
- Acetaminophen, Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Pain Relief NDC 0113-0025
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Anti Diarrheal Anti Gas NDC 0113-0087
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Migraine Formula NDC 0113-0374
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief NDC 0113-0403
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nighttime Sleep Aid NDC 0113-0431
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief Pm Extra Strength NDC 0113-0437
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Allergy Relief NDC 0113-0479
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief NDC 0113-0484
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0517
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief Arthritis Pain NDC 0113-0544
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0604
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0647
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-1019
- Generic Name
- Loratadine
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Anti Diarrheal Anti Gas NDC 0113-1087
- Generic Name
- Loperamide Hydrochloride, Simethicone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-1212
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Migraine Formula NDC 0113-1619
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Headache Relief NDC 0113-1855
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief NDC 0113-1889
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain Relief NDC 0113-1975
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Day Time Cold And Flu NDC 0113-4500
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Dual Action Back Pain NDC 0113-5299
- Generic Name
- Acetaminophen, Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugTemodar NDC 0085-1366
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1381
- Generic Name
- Temozolomide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1417
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1425
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1430
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1519
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-3004
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugUribel Tabs NDC 0178-0745
- Generic Name
- Methenamine, Benzoic Acid, Phenyl Salicylate, Methylene Blue...
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTegretol NDC 0078-0509
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0510
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0511
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0512
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Avo Spf35 NDC 0096-0687
- Generic Name
- Solbar Avo Spf35
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 35 Avo NDC 0096-0690
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 50 Fifty NDC 0096-0693
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Fifty Spf50 NDC 0096-0741
- Generic Name
- Solbar Fifty Spf50
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAldactone NDC 0025-1001
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1031
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1041
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugRasagiline NDC 0093-3060
- Generic Name
- Rasagiline
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugRasagiline NDC 0093-3061
- Generic Name
- Rasagiline
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSulfasalazine NDC 0093-3234
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugReclipsen 28 Day NDC 0093-3304
- Generic Name
- Desogestrel And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylergonovine Maleate NDC 0093-3655
- Generic Name
- Methylergonovine Maleate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 0093-7909
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugPacerone NDC 0245-0144
- Generic Name
- Amiodarone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPacerone NDC 0245-0147
- Generic Name
- Amiodarone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0245-0410
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0245-0411
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0245-0412
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
