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"31722-008-05" National Drug Code (NDC)

Zafirlukast 500 TABLET, FILM COATED in 1 BOTTLE (31722-008-05)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-008-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (31722-008-05)
Product NDC31722-008
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZafirlukast
Non-Proprietary NameZafirlukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200910
Marketing Category NameANDA
Application NumberANDA212475
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameZAFIRLUKAST
Strength20
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C9 Inhibitors [MoA], Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/31722-008-05





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