"70771-1703-5" National Drug Code (NDC)

Famotidine 500 TABLET, FILM COATED in 1 BOTTLE (70771-1703-5)
(Zydus Lifesciences Limited)

NDC Code70771-1703-5
Package Description500 TABLET, FILM COATED in 1 BOTTLE (70771-1703-5)
Product NDC70771-1703
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220606
Marketing Category NameANDA
Application NumberANDA216441
ManufacturerZydus Lifesciences Limited
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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