"68084-059-21" National Drug Code (NDC)

Zafirlukast 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-059-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-059-11)
(American Health Packaging)

NDC Code68084-059-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-059-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-059-11)
Product NDC68084-059
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZafirlukast
Non-Proprietary NameZafirlukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130603
Marketing Category NameANDA
Application NumberANDA090372
ManufacturerAmerican Health Packaging
Substance NameZAFIRLUKAST
Strength20
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C9 Inhibitors [MoA], Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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