"63629-7321-1" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (63629-7321-1)
(Bryant Ranch Prepack)

NDC Code63629-7321-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (63629-7321-1)
Product NDC63629-7321
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerBryant Ranch Prepack
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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