"71821-012-09" National Drug Code (NDC)

Famotidine 288461 TABLET, FILM COATED in 1 BAG (71821-012-09)
(VKT Pharma Private Limited)

NDC Code71821-012-09
Package Description288461 TABLET, FILM COATED in 1 BAG (71821-012-09)
Product NDC71821-012
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240523
Marketing Category NameANDA
Application NumberANDA215822
ManufacturerVKT Pharma Private Limited
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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