"63629-1014-3" National Drug Code (NDC)

Famotidine 300 TABLET in 1 BOTTLE (63629-1014-3)
(Bryant Ranch Prepack)

NDC Code63629-1014-3
Package Description300 TABLET in 1 BOTTLE (63629-1014-3)
Product NDC63629-1014
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerBryant Ranch Prepack
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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