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"72789-052-30" National Drug Code (NDC)
Ketoconazole 30 TABLET in 1 BOTTLE, PLASTIC (72789-052-30)
(PD-Rx Pharmaceuticals, Inc.)
NDC Code
72789-052-30
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (72789-052-30)
Product NDC
72789-052
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ketoconazole
Non-Proprietary Name
Ketoconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180626
Marketing Category Name
ANDA
Application Number
ANDA210457
Manufacturer
PD-Rx 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/72789-052-30