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"70518-0762-0" National Drug Code (NDC)
Ketoconazole 1 TUBE in 1 CARTON (70518-0762-0) > 30 g in 1 TUBE
(REMEDYREPACK INC.)
NDC Code
70518-0762-0
Package Description
1 TUBE in 1 CARTON (70518-0762-0) > 30 g in 1 TUBE
Product NDC
70518-0762
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ketoconazole
Non-Proprietary Name
Ketoconazole
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20171006
Marketing Category Name
ANDA
Application Number
ANDA075638
Manufacturer
REMEDYREPACK INC.
Substance Name
KETOCONAZOLE
Strength
20
Strength Unit
mg/g
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/70518-0762-0