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"71335-0439-7" National Drug Code (NDC)

Ketoconazole 14 TABLET in 1 BOTTLE (71335-0439-7)
(Bryant Ranch Prepack)

NDC Code71335-0439-7
Package Description14 TABLET in 1 BOTTLE (71335-0439-7)
Product NDC71335-0439
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKetoconazole
Non-Proprietary NameKetoconazole
Dosage FormTABLET
UsageORAL
Start Marketing Date19990615
Marketing Category NameANDA
Application NumberANDA075319
ManufacturerBryant Ranch Prepack
Substance NameKETOCONAZOLE
Strength200
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0439-7





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