NDC 58602-705

Famotidine

Famotidine

Famotidine is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Aurohealth Llc. The primary component is Famotidine.

Product ID58602-705_080b0f5f-a98c-4dc7-8183-0eff5cd51f7f
NDC58602-705
Product TypeHuman Otc Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-04-26
Marketing CategoryANDA / ANDA
Application NumberANDA206531
Labeler NameAurohealth LLC
Substance NameFAMOTIDINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58602-705-09

3 BLISTER PACK in 1 CARTON (58602-705-09) > 10 TABLET, FILM COATED in 1 BLISTER PACK (58602-705-03)
Marketing Start Date2016-04-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58602-705-15 [58602070515]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-19 [58602070519]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-12 [58602070512]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-03 [58602070503]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-09 [58602070509]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-93 [58602070593]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-26

NDC 58602-705-14 [58602070514]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-21

NDC 58602-705-84 [58602070584]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206531
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-13

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:756c7234-6a63-4b1b-be36-2b1ed09e67a0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199047
    • UPC Code
  • 0358602705190
  • 0358602705091

    • 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.