NDC 60429-721

Famotidine

Famotidine

Famotidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Golden State Medical Supply, Inc.. The primary component is Famotidine.

Product ID60429-721_7ceb98a1-0279-ddd6-e053-2991aa0a085d
NDC60429-721
Product TypeHuman Prescription Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2001-04-16
Marketing CategoryANDA / ANDA
Application NumberANDA075805
Labeler NameGolden State Medical Supply, Inc.
Substance NameFAMOTIDINE
Active Ingredient Strength40 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60429-721-01

100 TABLET in 1 BOTTLE (60429-721-01)
Marketing Start Date2011-12-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60429-721-10 [60429072110]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA075805
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-12-20
Marketing End Date2016-12-30

NDC 60429-721-01 [60429072101]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA075805
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-12-20

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE40 mg/1

OpenFDA Data

SPL SET ID:a526ee23-eb4b-4bf4-a815-61ae171d182b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310273
  • 284245
  • Pharmacological Class

    • Histamine H2 Receptor Antagonists [MoA]
    • Histamine-2 Receptor Antagonist [EPC]

    NDC Crossover Matching brand name "Famotidine" or generic name "Famotidine"

    NDCBrand NameGeneric Name
    0093-2748FamotidineFamotidine
    0172-5728FamotidineFamotidine
    0172-5729FamotidineFamotidine
    0338-5197FamotidineFamotidine
    0363-0036FamotidineFamotidine
    0363-1899FamotidineFamotidine
    68001-240FamotidineFamotidine
    68001-241FamotidineFamotidine
    68071-1879FamotidineFamotidine
    68071-3181FamotidineFamotidine
    68071-1941FamotidineFamotidine
    68071-3305FamotidineFamotidine
    68071-4197FamotidineFamotidine
    68071-3201FamotidineFamotidine
    68151-0184FamotidineFamotidine
    68151-0185FamotidineFamotidine
    68180-150FamotidineFamotidine
    68210-0007FAMOTIDINEFAMOTIDINE
    68382-444FamotidineFamotidine
    68645-140FamotidineFamotidine
    68645-141FamotidineFamotidine
    68788-6859FamotidineFamotidine
    68788-6399FamotidineFamotidine
    68788-9217FamotidineFamotidine
    68788-7191FamotidineFamotidine
    68788-9549FamotidineFamotidine
    68788-9220FamotidineFamotidine
    68788-9779FamotidineFamotidine
    70253-128FamotidineFamotidine
    70518-0460FamotidineFamotidine
    70518-0461FamotidineFamotidine
    70518-0163FamotidineFamotidine
    70518-1415FamotidineFamotidine
    70518-1341FamotidineFamotidine
    70518-1001FamotidineFamotidine
    70518-1089FamotidineFamotidine
    70518-1877FamotidineFamotidine
    71335-0409FamotidineFamotidine
    0615-4582FamotidineFamotidine
    71335-0370FamotidineFamotidine
    0615-4594FamotidineFamotidine
    72036-026FamotidineFamotidine
    0641-6023FamotidineFamotidine
    0641-6022FamotidineFamotidine
    0641-6021FamotidineFamotidine
    10544-481FamotidineFamotidine
    12634-967FamotidineFamotidine
    15127-370FamotidineFamotidine
    33261-185FamotidineFamotidine
    33261-562FamotidineFamotidine

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.