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"0093-0900-05" National Drug Code (NDC)

Ketoconazole 500 TABLET in 1 BOTTLE (0093-0900-05)
(Teva Pharmaceuticals USA Inc)

NDC Code0093-0900-05
Package Description500 TABLET in 1 BOTTLE (0093-0900-05)
Product NDC0093-0900
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKetoconazole
Non-Proprietary NameKetoconazole
Dosage FormTABLET
UsageORAL
Start Marketing Date19990615
Marketing Category NameANDA
Application NumberANDA075273
ManufacturerTeva Pharmaceuticals USA Inc
Substance NameKETOCONAZOLE
Strength200
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC],Azoles [Chemical/Ingredient],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/0093-0900-05





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