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"68788-9708-1" National Drug Code (NDC)
Ketoconazole 10 TABLET in 1 BOTTLE (68788-9708-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-9708-1
Package Description
10 TABLET in 1 BOTTLE (68788-9708-1)
Product NDC
68788-9708
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ketoconazole
Non-Proprietary Name
Ketoconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130205
Marketing Category Name
ANDA
Application Number
ANDA075319
Manufacturer
Preferred 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/68788-9708-1