NDC 64679-972

FAMOTIDINE

Famotidine

FAMOTIDINE is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Famotidine.

Product ID64679-972_28e963b7-6088-45ba-b030-8cb6cfcd84f0
NDC64679-972
Product TypeHuman Otc Drug
Proprietary NameFAMOTIDINE
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-03-07
Marketing CategoryANDA / ANDA
Application NumberANDA077146
Labeler NameWockhardt USA LLC.
Substance NameFAMOTIDINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 64679-972-00

50000 TABLET in 1 DRUM (64679-972-00)
Marketing Start Date2005-03-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-972-02 [64679097202]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA077146
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-03-07

NDC 64679-972-00 [64679097200]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA077146
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-03-07

NDC 64679-972-01 [64679097201]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA077146
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-03-07

NDC 64679-972-03 [64679097203]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA077146
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-03-07

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:fe1b437a-07de-4d5a-aa95-955e849dc6d6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199047
  • 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.