"71821-010-12" National Drug Code (NDC)

Famotidine 144230 TABLET, FILM COATED in 1 BAG (71821-010-12)
(VKT Pharma Private Limited)

NDC Code71821-010-12
Package Description144230 TABLET, FILM COATED in 1 BAG (71821-010-12)
Product NDC71821-010
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220128
Marketing Category NameANDA
Application NumberANDA215822
ManufacturerVKT Pharma Private Limited
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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