NDC 55648-374

FAMOTIDINE

Famotidine

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

Product ID55648-374_d0e9c888-c641-40a8-9338-d83b6de02385
NDC55648-374
Product TypeHuman Otc Drug
Proprietary NameFAMOTIDINE
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-08-06
Marketing CategoryANDA / ANDA
Application NumberANDA090837
Labeler NameWOCKHARDT LIMITED
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 55648-374-00

38000 TABLET in 1 DRUM (55648-374-00)
Marketing Start Date2010-08-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55648-374-09 [55648037409]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-08-07
Inactivation Date2019-11-13

NDC 55648-374-08 [55648037408]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-08-06
Inactivation Date2019-11-13

NDC 55648-374-05 [55648037405]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-08-06
Inactivation Date2019-11-13

NDC 55648-374-00 [55648037400]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-08-06
Inactivation Date2019-11-13

NDC 55648-374-07 [55648037407]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-08-06
Inactivation Date2019-11-13

NDC 55648-374-01 [55648037401]

FAMOTIDINE TABLET
Marketing CategoryANDA
Application NumberANDA090837
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-08-06
Inactivation Date2019-11-13

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

OpenFDA Data

SPL SET ID:fdff466f-9884-4bbd-89af-0e186a54801b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310273
    • UPC Code
  • 0364679374054

    • 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
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