NDC 55111-396

Famotidine

Famotidine

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

Product ID55111-396_0e165efa-c6cc-c254-e143-a757293c26b3
NDC55111-396
Product TypeHuman Otc Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-09-30
Marketing CategoryANDA / ANDA
Application NumberANDA077367
Labeler NameDr.Reddys Laboratories Limited
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 55111-396-08

1 BLISTER PACK in 1 CARTON (55111-396-08) > 8 TABLET in 1 BLISTER PACK
Marketing Start Date2006-09-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55111-396-44 [55111039644]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-01 [55111039601]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-32 [55111039632]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-08 [55111039608]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-50 [55111039650]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-35 [55111039635]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

NDC 55111-396-16 [55111039616]

Famotidine TABLET
Marketing CategoryANDA
Application NumberANDA077367
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-09-30

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

OpenFDA Data

SPL SET ID:387088a6-8eaa-fc49-8050-a546d0f0fd32
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199047
  • 310273

    • 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.