Ketodan - 43538-530-10 - (ketoconazole)

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Drug Information of Ketodan

Product NDC: 43538-530
Proprietary Name: Ketodan
Non Proprietary Name: ketoconazole
Active Ingredient(s): 20    mg/g & nbsp;   ketoconazole
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of Ketodan

Product NDC: 43538-530
Labeler Name: Medimetriks Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091550
Marketing Category: ANDA
Start Marketing Date: 20120615

Package Information of Ketodan

Package NDC: 43538-530-10
Package Description: 1 CAN in 1 CARTON (43538-530-10) > 100 g in 1 CAN

NDC Information of Ketodan

NDC Code 43538-530-10
Proprietary Name Ketodan
Package Description 1 CAN in 1 CARTON (43538-530-10) > 100 g in 1 CAN
Product NDC 43538-530
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketoconazole
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20120615
Marketing Category Name ANDA
Labeler Name Medimetriks Pharmaceuticals, Inc.
Substance Name KETOCONAZOLE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Ketodan


General Information