"72162-2361-6" National Drug Code (NDC)

Zafirlukast 60 TABLET, FILM COATED in 1 BOTTLE (72162-2361-6)
(Bryant Ranch Prepack)

NDC Code72162-2361-6
Package Description60 TABLET, FILM COATED in 1 BOTTLE (72162-2361-6)
Product NDC72162-2361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZafirlukast
Non-Proprietary NameZafirlukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200910
Marketing Category NameANDA
Application NumberANDA212475
ManufacturerBryant Ranch Prepack
Substance NameZAFIRLUKAST
Strength20
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C9 Inhibitors [MoA], Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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