NDC 11673-031

up and up famotidine

Famotidine

up and up famotidine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Famotidine.

Product ID11673-031_0d6f2ac0-295e-47ce-aedb-8cadc1e66a63
NDC11673-031
Product TypeHuman Otc Drug
Proprietary Nameup and up famotidine
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-03-13
Marketing CategoryANDA / ANDA
Application NumberANDA075400
Labeler NameTarget Corporation
Substance NameFAMOTIDINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 11673-031-65

30 BLISTER PACK in 1 CARTON (11673-031-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2015-03-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-031-65 [11673003165]

up and up famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075400
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-03-13

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:0d6f2ac0-295e-47ce-aedb-8cadc1e66a63
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199047
  • NDC Crossover Matching brand name "up and up famotidine" or generic name "Famotidine"

    NDCBrand NameGeneric Name
    11673-061up and up famotidineup and up famotidine
    11673-031up and up famotidineup and up famotidine
    0363-0141Acid ControllerFamotidine
    0363-0701Acid ControllerFamotidine
    0363-1203acid controllerfamotidine
    0113-7141basic care acid reducerFamotidine
    0113-7194Basic Care famotidineFamotidine
    0093-2748FamotidineFamotidine
    0172-5728FamotidineFamotidine
    0172-5729FamotidineFamotidine
    0338-5197FamotidineFamotidine
    0363-0036FamotidineFamotidine
    0363-1899FamotidineFamotidine
    0113-0141good sense acid reducerFamotidine
    0113-0194Good Sense Acid ReducerFamotidine
    0187-4420Pepcidfamotidine
    0187-4440Pepcidfamotidine

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