NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 50090-5179
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Inhalant
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Oleic Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 2UMI9U37CP.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 112-80-1 and the RxNorm Concept ID (RxCUI) 7631. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
OLEIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
2UMI9U37CP
The specific atomic composition represented as a molecular structure string.
InChIKey
C18H34O2 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
ZQPPMHVWECSIRJ-KTKRTIGZSA-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
CCCCCCCC/C=C\CCCCCCCC(=O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Oleic 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
OLEIC ACID
OF
Common Names & Synonyms
9-OCTADECENOIC ACID, (Z)-
CN
9Z-OCTADECENOIC ACID
CN
ENDOCINE COMPONENT OLEIC ACID
CN
OLEIC ACID (C18:1) (CONSTITUENT OF KRILL OIL) [DSC]
CN
OLEIC ACID (CONSTITUENT OF BORAGE SEED OIL) [DSC]
CN
OLEIC ACID (CONSTITUENT OF EVENING PRIMROSE OIL) [DSC]
CN
OLEIC ACID (CONSTITUENT OF FLAX SEED OIL) [DSC]
CN
OLEIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]
CN
OLEIC ACID (CONSTITUENT OF SPIRULINA) [DSC]
CN
OLEIC ACID [EP MONOGRAPH]
CN
OLEIC ACID [FCC]
CN
OLEIC ACID [FHFI]
CN
OLEIC ACID [HSDB]
CN
OLEIC ACID [II]
CN
OLEIC ACID [MART.]
CN
OLEIC ACID [MI]
CN
OLEIC ACID [USP-RS]
CN
OLEIC ACID [VANDF]
CN
OLEIC ACID [WHO-DD]
CN
OSTEUM
CN
PRIOLENE 6936
CN
VOPCOLENE 27
CN
WECOLINE OO
CN
Systematic Nomenclature
9-OCTADECENOIC ACID (9Z)-
SYS
CIS-9-OCTADECENOIC ACID
SYS
OLEATE
SYS
Technical Codes
18:1(N-9)
CD
FEMA NO. 2815
CD
NSC-9856
CD
NDC Products Containing OLEIC 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 (376), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 50090-5735
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Inhalant
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugCarbamazepine NDC 62559-484
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 62559-485
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 62559-486
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugLevalbuterol Tartrate Hfa Inhalation NDC 0591-2927
- Generic Name
- Levalbuterol Tartrate
- Dosage Form
- Aerosol, Metered
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate NDC 45963-303
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate NDC 45963-304
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate NDC 45963-305
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advagen Pharma Ltd
NDC Product
Human Prescription DrugTopiramate NDC 72888-228
- Generic Name
- Topiramate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 72888-229
- Generic Name
- Topiramate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aekyung Industrial Co., Ltd.
NDC Product
Human Otc DrugAge20s Uv Defense Hydro Calming Sunscreen NDC 67225-5033
- Generic Name
- Octocrylene, Homosalate, Octisalate, Avobenzone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAge20s Uv Defense Hydro Calming Sunscreen Twin Pack NDC 67225-5034
- Generic Name
- Octocrylene, Homosalate, Octisalate, Avobenzone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAge20s Sunscreen Duo NDC 67225-5333
- Generic Name
- Zinc Oxide, Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 27241-191
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 27241-192
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-227
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-228
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-229
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 27241-230
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugNamzaric NDC 0456-1207
- Generic Name
- Memantine Hydrochloride And Donepezil Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNamzaric NDC 0456-1214
- Generic Name
- Memantine Hydrochloride And Donepezil Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNamzaric NDC 0456-1221
- Generic Name
- Memantine Hydrochloride And Donepezil Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNamzaric NDC 0456-1228
- Generic Name
- Memantine Hydrochloride And Donepezil Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Allure Labs
NDC Product
Human Otc DrugOs-01 Lip Spf Bs Spf15 NDC 62742-4270
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
American Health Packaging
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 60687-319
- Generic Name
- Tolterodine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 60687-330
- Generic Name
- Tolterodine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 60687-662
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Inhalant
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71610-030
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 71610-688
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71610-707
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugTopiramate NDC 42291-955
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-956
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-957
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-958
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Beiersdorf Inc
NDC Product
Human Otc DrugEucerin Eczema Relief Hydrogel NDC 10356-390
- Generic Name
- Oatmeal
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCoppertone Every Tone Face Hydrating Clear Sunscreen Spf 60 NDC 66800-8001
- Generic Name
- Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCoppertone Every Tone Invisible Clear Sunscreen Stick Spf 55 NDC 66800-8003
- Generic Name
- Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 10...
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Best Sanitizers, Inc
NDC Product
Human Otc DrugSoftensure Antimicrobial Liquid NDC 59900-217
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Blistex Inc
NDC Product
Human Otc DrugBlistex Medicated Lip Balm Variety Pack (blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Lip) NDC 10157-9910
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Camphor (synthetic), Me...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Blistex Inc.
NDC Product
Human Otc DrugBlistex Medicated NDC 10157-9951
- Generic Name
- Dimethicone, Camphor (synthetic), Menthol, And Phenol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bobbi Brown Professional Cosmetics Inc.
NDC Product
Human Otc DrugBobbi Brown Lip Balm Broad Spectrum Spf 15 NDC 64141-019
- Generic Name
- Avobenzone, Octinoxate, And Octisalate
- Dosage Form
- Lipstick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugMometasone Furoate NDC 63629-8685
- Generic Name
- Mometasone Furoate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMometasone Furoate NDC 63629-8686
- Generic Name
- Mometasone Furoate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 71335-2725
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 71335-3000
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMometasone Furoate NDC 72162-1392
- Generic Name
- Mometasone Furoate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 72162-2332
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Buckeye International, Inc.
NDC Product
Human Otc DrugSymmetry Antimicrobial Foaming Hand Wash NDC 30805-006
- Generic Name
- Chloroxylenol
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAltra Antimicrobial Foaming Hand Wash With 0.3% Pcmx NDC 30805-016
- Generic Name
- Chloroxylenol
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugTopiramate NDC 31722-547
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-548
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-549
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 31722-550
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cipla USA Inc.
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 69097-142
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Inhalant
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Cosmetic Enterprise Ltd
NDC Product
Human Otc DrugAnti Bac Acne Clearing NDC 56152-4012
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Coupler LLC
NDC Product
Human Prescription DrugCarbamazepine NDC 67046-1455
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 67046-1558
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 67046-1559
- Generic Name
- Carbamazepine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Human Prescription DrugImiquimod NDC 72189-084
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
DUKE CANNON SUPPLY CO.
NDC Product
Human Otc DrugCannon Balm 140 NDC 71782-141
- Generic Name
- Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Human Prescription DrugVenlafaxine NDC 43598-943
- Generic Name
- Venlafaxine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVenlafaxine NDC 43598-944
- Generic Name
- Venlafaxine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy�s Laboratories Inc.
NDC Product
Human Prescription DrugTopiramate NDC 43598-939
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 43598-940
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 43598-941
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 43598-942
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dynarex Corporation
NDC Product
Human Otc DrugDynarex Green NDC 67777-308
- Generic Name
- Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
ENGLEWOOD LAB, INC.
NDC Product
Human Otc DrugByoma Moisturizing Gel Sunscreen Broad Spectrum Spf 30 NDC 14268-123
- Generic Name
- Avobenzone, Homosalate, Octisalate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
ESTEE LAUDER INC
NDC Product
Human Otc Drug- Generic Name
- Ensulizole, Octinoxate, Octisalate, And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Eden Brands Inc.
NDC Product
Human Otc DrugEvereden Intensive Eczema Balm NDC 72113-109
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Fresenius Kabi Austria GmbH
NDC Product
Human Prescription DrugCleviprex NDC 18124-011
- Generic Name
- Clevidipine
- Dosage Form
- Emulsion
- Route
- Intravenous
- Marketing
- NDA
Active Listing
GOJO INDUSTRIES, INC.
NDC Product
Human Otc DrugMicrell Antibacterial Ltn Sp NDC 21749-975
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
GOJO Industries, Inc.
NDC Product
Human Otc DrugGojo Rich Pink Antibacterial Ltn Sp NDC 21749-060
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGojo Ultra Mild Antimicrobial Ltn Sp With Chloroxylenol NDC 21749-211
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPurell Healthy Sp Antibacterial Ltn Sp With Pcmx NDC 21749-423
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGojo Pcmx E-2 Sanitizing Ltn Sp NDC 21749-457
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGojo Antibacterial Ltn Sp NDC 21749-458
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGojo Gold And Klean Antimicrobial Ltn Sp NDC 21749-501
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugProvon Antimicrobial Ltn Sp With 0.3% Pcmx NDC 21749-750
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Glenmark Pharmaceuticals Inc., USA
NDC Product
Human Prescription DrugTretinoin NDC 68462-792
- Generic Name
- Tretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 51407-059
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Guinot
NDC Product
Human Otc DrugSun Logic Lait Solaire Corps Spf 20 NDC 54181-010
- Generic Name
- Avobenzone, Homosalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 0054-0742
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Hisamitsu America, Inc.
NDC Product
Human Otc DrugSalonpas Lidocaine Pain Relieving NDC 55328-100
- Generic Name
- Lidocaine
- Dosage Form
- Patch
- Route
- Percutaneous; Topical; Transdermal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hisamitsu Pharmaceutical Co., Inc.
NDC Product
Human Otc DrugSalonpas Lidocaine Pain Relieving NDC 46581-830
- Generic Name
- Lidocaine
- Dosage Form
- Patch
- Route
- Percutaneous; Topical; Transdermal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hisun Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugLevetiracetam NDC 42658-148
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevetiracetam NDC 42658-149
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Industria La Popular, S.A.
NDC Product
Human Otc DrugDk12 Shower Gel Creamy NDC 62476-010
- Generic Name
- Benzalkonium Chloride 0.13%
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDk12 Shower Gel Fresh Energy NDC 62476-011
- Generic Name
- Benzalkonium Chloride 0.13%
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
June Jacobs Labs LLC
NDC Product
Human Otc DrugRapid Repair Healing Cream NDC 65278-110
- Generic Name
- Allantoin, Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kao USA Inc
NDC Product
Human Otc Drug- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBan Invisible Solid Antiperspirant Deodorant Unscented NDC 10596-335
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kao USA Inc.
NDC Product
Human Otc Drug- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kingsway Pharmaceuticals dba NFI, LLC
NDC Product
Human Otc DrugMaximum Strength Blue Emu Pain Relief Blu Emu NDC 69993-100
- Generic Name
- Trolamine Salicylate
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugXopenex Hfa NDC 27437-056
- Generic Name
- Levalbuterol Tartrate
- Dosage Form
- Aerosol, Metered
- Route
- Oral
- Marketing
- NDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugIsentress NDC 0006-0473
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0477
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3080
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3603
- Generic Name
- Raltegravir
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Murad, LLC
NDC Product
Human Otc DrugMulti Vitamin Clear Coat Broad Spectrum Spf 50 NDC 70381-125
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mylan Institutional Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 51079-766
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 51079-767
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 51079-917
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0378-0472
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0378-0473
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 0378-6320
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 0378-6380
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 0378-6440
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Natureteq Inc.
NDC Product
Human Otc DrugMedistik Professional Dual Action NDC 50231-221
- Generic Name
- Menthol, Methyl Salicylate, Eucaluptus
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Noven Therapeutics, LLC
NDC Product
Human Prescription Drug- Generic Name
- Estradiol/norethindrone Acetate Transdermal System
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Estradiol/norethindrone Acetate Transdermal System
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- NDA
Active Listing
PARMA KOREA
NDC Product
Human Otc DrugParma Anus Skin Premium Cleanser NDC 71614-002
- Generic Name
- Allantoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Padagis Israel Pharmaceuticals Ltd
NDC Product
Human Prescription DrugMometasone Furoate NDC 45802-118
- Generic Name
- Mometasone Furoate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 45802-368
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Praxis, LLC
NDC Product
Human Prescription DrugLevalbuterol Tartrate Hfa Inhalation NDC 59368-410
- Generic Name
- Levalbuterol Tartrate
- Dosage Form
- Aerosol, Metered
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 68788-7996
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 68788-8787
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 68788-8874
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Inhalant
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugLevalbuterol Tartrate Hfa Inhalation NDC 63187-876
- Generic Name
- Levalbuterol Tartrate
- Dosage Form
- Aerosol, Metered
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
RB Health (US) LLC
NDC Product
Human Otc DrugBiofreeze Dry Stick NDC 59316-230
- Generic Name
- Menthol
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMucinex Sinus Max Clear And Cool Severe Congestion NDC 72854-218
- Generic Name
- Oxymetazoline Hci
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 70518-4528
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Revlon Consumer Products Corp
NDC Product
Human Otc DrugRevlon Photoready Insta-fix Makeup NDC 10967-631
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rodan & Fields
NDC Product
Human Otc DrugUnblemish Invisible Matte Defense NDC 14222-2131
- Generic Name
- Homosalate, Octocrylene, Octisalate, Avobenzone
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugUnblemish 30-day Regimen NDC 14222-2150
- Generic Name
- Salicylic Acid, Benzoyl Peroxide, Homosalate, Octocrylene, O...
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoothe Sensitive Skin Treatment NDC 14222-2420
- Generic Name
- Allantoin, Dimethicone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRodan And Fields Plumping Lip Spf 28 Sunscreen NDC 14222-3000
- Generic Name
- Octinoxate, Zinc Oxide
- Dosage Form
- Oil
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SJ Bio Co., Ltd.
NDC Product
Human Otc DrugOdeur Senior Premium Cleanser NDC 69798-001
- Generic Name
- Menthol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugOdeur Premium Body Cleanser NDC 69798-002
- Generic Name
- Menthol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Safecor Health, LLC
NDC Product
Human Prescription DrugDivalproex Sodium NDC 48433-033
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 48433-034
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugAlbuterol Sulfate NDC 0781-7296
- Generic Name
- Albuterol Sulfate
- Dosage Form
- Aerosol, Metered
- Route
- Respiratory (inhalation)
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Slate Run Pharmaceuticals, LLC
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 70436-054
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 70436-055
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 70436-056
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 70436-057
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 70436-160
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 70436-161
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-0127
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-0136
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-0154
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0803
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0804
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0805
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0807
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1810
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1820
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1830
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1840
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1850
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride Extended-release NDC 0406-1860
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8960
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8961
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8962
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Bum, LLC
NDC Product
Human Otc DrugSun Bum High Performance Sunscreen Signature Clear 50 NDC 69039-707
- Generic Name
- Octocrylene, Octisalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octocrylene, Octisalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octisalate, Octocrylene, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Supernus Pharmaceuticals, Inc
NDC Product
Human Prescription DrugQelbree NDC 17772-131
- Generic Name
- Viloxazine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQelbree NDC 17772-132
- Generic Name
- Viloxazine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQelbree NDC 17772-133
- Generic Name
- Viloxazine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Supernus Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-101
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-102
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-103
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTrokendi Xr NDC 17772-104
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TARO PHARMACEUTICALS U.S.A., INC.
NDC Product
Human Otc DrugBebe Bottoms NDC 51672-5318
- Generic Name
- Zinc Oxide
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TOLMAR Inc.
NDC Product
Human Prescription DrugJatenzo NDC 69087-158
- Generic Name
- Testosterone Undecanoate
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJatenzo NDC 69087-198
- Generic Name
- Testosterone Undecanoate
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJatenzo NDC 69087-237
- Generic Name
- Testosterone Undecanoate
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugTopiramate NDC 0480-2359
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Tommie Copper, Inc.
NDC Product
Human Otc DrugCopperlife Foot NDC 72562-211
- Generic Name
- Dimethicone 1%
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTommie Copper Foot NDC 72562-222
- Generic Name
- Dimethicone 1%
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 13668-189
- Generic Name
- Tolterodine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 13668-190
- Generic Name
- Tolterodine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Uriel Pharmacy Inc.
NDC Product
Human Otc DrugResina Laricis Bath Milk NDC 48951-8326
- Generic Name
- Resina Laricis Bath Milk
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
VGYAAN Pharmaceuticals LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 72664-227
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 72664-228
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Veridian Healthcare
NDC Product
Human Otc DrugTheracare Pain Relief Patch NDC 71101-108
- Generic Name
- Lidocaine 4%
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Vitruvias Therapeutics, Inc.
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 69680-161
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 69680-162
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMemantine Hydrochloride NDC 69680-164
- Generic Name
- Memantine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
W.W. GRAINGER, INC.
NDC Product
Human Otc DrugTough Guy 821 Antimicrobial Liquid Ltion So Ap NDC 40096-0051
- Generic Name
- Chloroxylenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Westminster Pharmaceuticals, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 69367-412
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 69367-413
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugEstradiol NDC 70771-1563
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70771-1564
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70771-1565
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70771-1566
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70771-1567
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugEstradiol NDC 70710-1191
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70710-1192
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70710-1193
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70710-1194
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 70710-1195
- Generic Name
- Estradiol
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
