NDC 11673-414

up and up famotidine

Famotidine

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

Product ID11673-414_4ab1b57d-0782-4882-a144-3c96cfe05fad
NDC11673-414
Product TypeHuman Otc Drug
Proprietary Nameup and up famotidine
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-01-25
Marketing CategoryANDA /
Application NumberANDA077351
Labeler NameTarget Corporation
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 11673-414-63

1 BOTTLE in 1 CARTON (11673-414-63) > 25 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2022-01-25
NDC Exclude FlagN
Sample Package?N

Drug Details

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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