"11673-031-72" National Drug Code (NDC)

Up And Up Famotidine 1 BOTTLE in 1 CARTON (11673-031-72) > 60 TABLET, FILM COATED in 1 BOTTLE
(Target Corporation)

NDC Code11673-031-72
Package Description1 BOTTLE in 1 CARTON (11673-031-72) > 60 TABLET, FILM COATED in 1 BOTTLE
Product NDC11673-031
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Famotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150313
Marketing Category NameANDA
Application NumberANDA075400
ManufacturerTarget Corporation
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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