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"68071-4012-3" National Drug Code (NDC)
Ketoconazole 30 TABLET in 1 BOTTLE (68071-4012-3)
(NuCare Pharmaceuticals, Inc.)
NDC Code
68071-4012-3
Package Description
30 TABLET in 1 BOTTLE (68071-4012-3)
Product NDC
68071-4012
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
ANDA075319
Manufacturer
NuCare Pharmaceuticals, 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/68071-4012-3