NDC Product
Drug For Further Processing- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Sodium Benzoate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) OJ245FE5EU.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 532-32-1 and the RxNorm Concept ID (RxCUI) 56455. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SODIUM BENZOATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
OJ245FE5EU
The specific atomic composition represented as a molecular structure string.
InChIKey
C7H5O2.Na International Chemical Identifier digital signature for unique molecular identification.
SMILES String
WXMKPNITSTVMEF-UHFFFAOYSA-M Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
USAN ID
AA-68
Identifier assigned by the United States Adopted Names Council.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C([O-])(=O)c1ccccc1.[Na+]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Sodium Benzoate. 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
SODIUM BENZOATE
OF
Common Names & Synonyms
AMMONUL COMPONENT SODIUM BENZOATE
CN
ANTIMOL
CN
FUMINARU
CN
MICROCARE SB
CN
PUROX S
CN
SOBENATE
CN
SODIUM BENZOATE [EP MONOGRAPH]
CN
SODIUM BENZOATE [FCC]
CN
SODIUM BENZOATE [FHFI]
CN
SODIUM BENZOATE [HSDB]
CN
SODIUM BENZOATE [II]
CN
SODIUM BENZOATE [JAN]
CN
SODIUM BENZOATE [MART.]
CN
SODIUM BENZOATE [MI]
CN
SODIUM BENZOATE [ORANGE BOOK]
CN
SODIUM BENZOATE [USAN]
CN
SODIUM BENZOATE [USP-RS]
CN
SODIUM BENZOATE [VANDF]
CN
SODIUM BENZOATE [WHO-DD]
CN
UCEPHAN COMPONENT SODIUM BENZOATE
CN
Technical Codes
E-211
CD
FEMA NO. 3025
CD
INS NO.211
CD
INS-211
CD
NDC Products Containing SODIUM BENZOATE
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
Actavis Pharma, Inc.
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-2027
- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-2029
- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-2031
- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-2039
- Generic Name
- Alprazolam
- Dosage Form
- Tablet
- 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 0187-3012
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Solution
- 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
Boiron
NDC Product
Human Otc DrugChestal Cold And Cough Honey NDC 0220-9121
- Generic Name
- Solanum Dulcamara Top, Ferrosoferric Phosphate, Goldenseal, ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal Kids Cold And Cough Honey NDC 0220-9122
- Generic Name
- Solanum Dulcamara Top, Ferrosoferric Phosphate, Goldenseal, ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugFleet NDC 0132-0401
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Colgate Oral Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPrevident Alcohol Free NDC 0126-0033
- Generic Name
- Sodium Fluoride
- Dosage Form
- Mouthwash
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident 5000 Plus Fruitastic NDC 0126-0286
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident 5000 Plus Spearmint NDC 0126-0287
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident Orthodefense NDC 0126-0289
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident 5000 Kids NDC 0126-0311
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugTamiflu NDC 0004-0822
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Cough Dm Day Night Value Pack NDC 0031-2059
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Value Pack NDC 0031-2099
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Chlorpheniramine...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Childrens Honey Day Night Dm Value Pack NDC 0031-2102
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Maximum Strength Cough Dm NDC 0031-2103
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Dm Max NDC 0031-2834
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough Long-acting NDC 0031-8694
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8702
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8715
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Cold Cf NDC 0031-8716
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Maximum Strength Nighttime Cough Dm NDC 0031-8718
- Generic Name
- Dextromethorphan Hydrobromide, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Bulk Ingredient- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hy...
- Dosage Form
- Syrup
- Route
- N/A
- Marketing
- EXPORT ONLY
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Peak Cold Multi-symptom Cold NDC 0031-8742
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu NDC 0031-8751
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu Nighttime NDC 0031-8752
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Cough Plus Chest Congestion Dm NDC 0031-8757
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Honey Cough And Chest Congestion Dm NDC 0031-8760
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Severe Cough, Flu Plus Sore Throat NDC 0031-8771
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Chest Congestion Daytime NDC 0067-0104
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-0105
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief NDC 0067-0107
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenphydramine Hcl, G...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Pseudoephedrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Nighttime Value Pack NDC 0067-8125
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl And A...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8127
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8129
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Syrup NDC 0067-8132
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Syrup
- 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 DrugEx-lax Maximum Strength Stimulant Laxative NDC 0067-8142
- Generic Name
- Sennosides
- Dosage Form
- Pill
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPerdiem NDC 0067-8143
- Generic Name
- Sennosides, Stimulant Laxative
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-8204
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-8205
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0183
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Tropical Fruit Smoothie NDC 0135-0185
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Raspberry Lemonade NDC 0135-0188
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Extreme Clean Whitening Action NDC 0135-0234
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Clean Mint NDC 0135-0449
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Extra Fresh NDC 0135-0451
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiotene NDC 0135-0577
- Generic Name
- Sodium Monofluorophosphate
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0606
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Peppermint NDC 0135-0623
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites With Gas Relief NDC 0135-0624
- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Mixed Fruit NDC 0135-0641
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugParodontax Active Gum Health Clear Mint NDC 0135-0650
- Generic Name
- Cetylpyridinium Chloride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugParodontax Active Gum Health Mint NDC 0135-0651
- Generic Name
- Cetylpyridinium Chloride
- Dosage Form
- Mouthwash
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Cetylpyridinium Chloride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0391
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0392
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugOndansetron Hydrochloride NDC 0054-0064
- Generic Name
- Ondansetron Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLinezolid NDC 0054-0319
- Generic Name
- Linezolid
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPosaconazole NDC 0054-0449
- Generic Name
- Posaconazole
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0517
- Generic Name
- Morphine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMeperidine Hydrochloride NDC 0054-3545
- Generic Name
- Meperidine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-3553
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidazolam Hydrochloride NDC 0054-3566
- Generic Name
- Midazolam Hydrochloride
- Dosage Form
- Syrup
- 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 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 DrugDoxycycline Hyclate NDC 0143-2112
- Generic Name
- Doxycycline Hyclate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0143-9886
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0143-9887
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0143-9888
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0143-9889
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmceuticals USA Inc.
NDC Product
Human Prescription DrugOxycodone Hydrochloride NDC 0054-0390
- Generic Name
- Oxycodone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
L Perrigo Company
NDC Product
Human Otc DrugMederma Pm NDC 0113-4124
- Generic Name
- Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Severe Nighttime NDC 0113-0019
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0020
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Infants NDC 0113-0057
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever NDC 0113-0161
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0166
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Time NDC 0113-0186
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens All Day Allergy NDC 0113-0189
- Generic Name
- Cetirizine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0212
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Allergy NDC 0113-0379
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens All Day Allergy NDC 0113-0503
- Generic Name
- Cetirizine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0608
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0660
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-0671
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0685
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Nighttime Cold And Flu NDC 0113-0763
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0897
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm Max NDC 0113-0927
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hemorrhoidal Maximum Strength Pain Relief NDC 0113-0944
- Generic Name
- Glycerin, Phenylephrine Hcl, Pramoxine Hcl, White Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever Infants NDC 0113-0946
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold And Cough NDC 0113-0987
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hbr, Phenylephrine...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Antidiarrheal NDC 0113-1645
- Generic Name
- Loperamide Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-1719
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm NDC 0113-1725
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin NDC 0113-2009
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Day Time Cold And Flu NDC 0113-2299
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time Cold And Flu NDC 0113-2501
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-6012
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold Cough NDC 0113-6019
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever NDC 0113-8959
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Laboratoires Boiron
NDC Product
Human Otc DrugChestal NDC 0220-9032
- Generic Name
- Antimony Potassium Tartrate, Bryonia Alba Root, Protortonia ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal For Children NDC 0220-9033
- Generic Name
- Antimony Potassium Tartrate, Bryonia Alba Root, Protortonia ...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal Cough And Cold NDC 0220-9067
- Generic Name
- Solanum Dulcamara Top, Ferrum Phosphoricum, Goldenseal, Pota...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChestal Childrens Cough And Cold NDC 0220-9068
- Generic Name
- Solanum Dulcamara Top, Ferrum Phosphoricum, Goldenseal, Pota...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugNoxafil NDC 0085-1328
- Generic Name
- Posaconazole
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-2224
- Generic Name
- Posaconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4324
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4331
- Generic Name
- Posaconazole
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
PAI Holdings, LLC
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-0775
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-1550
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-1775
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Otc DrugGuaifenesin Dm NDC 0121-0638
- Generic Name
- Guaifenesin And Dextromethorphan
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0121-0653
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-0657
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugEthosuximide NDC 0121-0670
- Generic Name
- Ethosuximide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Citrate And Citric Acid NDC 0121-0676
- Generic Name
- Potassium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTricitrates NDC 0121-0677
- Generic Name
- Potassium Citrate, Sodium Citrate, And Citric Acid Monohydra...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0121-0678
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-0744
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugOxycodone Hydrochloride NDC 0121-0827
- Generic Name
- Oxycodone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0833
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDiphenhydramine Hcl NDC 0121-0865
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugOndansetron NDC 0121-0882
- Generic Name
- Ondansetron
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenytoin NDC 0121-0892
- Generic Name
- Phenytoin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0121-0904
- Generic Name
- Morphine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-0941
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-0948
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDye Free Childrens Acetaminophen NDC 0121-0966
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDye Free Childrens Ibuprofen NDC 0121-1022
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 0121-1034
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1047
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPromethazine Dm NDC 0121-1070
- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin Dm NDC 0121-1276
- Generic Name
- Guaifenesin And Dextromethorphan
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1314
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-1488
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-1666
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDiphenhydramine Hcl NDC 0121-1730
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-1744
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Acetaminophen NDC 0121-1781
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1882
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-1896
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1971
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2094
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-2232
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2823
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-2847
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-3141
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugOxycodone Hydrochloride NDC 0121-4827
- Generic Name
- Oxycodone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-4948
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Par Health USA, LLC
NDC Product
Human Prescription DrugDiazoxide NDC 0254-1010
- Generic Name
- Diazoxide
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugZarontin NDC 0071-2418
- Generic Name
- Ethosuximide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugXeljanz NDC 0069-1029
- Generic Name
- Tofacitinib
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmaceutical Associates, Inc.
NDC Product
Human Prescription DrugSodium Citrate And Citric Acid NDC 0121-0595
- Generic Name
- Sodium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0914
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSodium Citrate And Citric Acid NDC 0121-1190
- Generic Name
- Sodium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2267
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2268
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4125
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4127
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4136
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4137
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-4155
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4175
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4177
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOseltamivir Phosphate NDC 0093-8180
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories Inc.
NDC Product
Human Prescription DrugValproic Acid NDC 0116-4021
- Generic Name
- Valproic Acid
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc
NDC Product
Human Prescription Drug- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Prescription DrugMegestrol Acetate NDC 0116-4011
- Generic Name
- Megestrol Acetate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0116-4023
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
