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"51672-4026-9" National Drug Code (NDC)

Ketoconazole 5 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACK
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-4026-9
Package Description5 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACK
Product NDC51672-4026
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKetoconazole
Non-Proprietary NameKetoconazole
Dosage FormTABLET
UsageORAL
Start Marketing Date19990615
Marketing Category NameANDA
Application NumberANDA075319
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
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]

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