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"0093-0900-01" National Drug Code (NDC)
Ketoconazole 100 TABLET in 1 BOTTLE (0093-0900-01)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0900-01
Package Description
100 TABLET in 1 BOTTLE (0093-0900-01)
Product NDC
0093-0900
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ketoconazole
Non-Proprietary Name
Ketoconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19990615
Marketing Category Name
ANDA
Application Number
ANDA075273
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
KETOCONAZOLE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Azole 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/0093-0900-01