"68071-3413-3" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (68071-3413-3)
(NuCare Pharmceuticals,Inc.)

NDC Code68071-3413-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-3413-3)
Product NDC68071-3413
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220708
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerNuCare Pharmceuticals,Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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