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ketoconazole - 52125-375-01 - (ketoconazole)

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Drug Information of ketoconazole

Product NDC: 52125-375
Proprietary Name: ketoconazole
Non Proprietary Name: ketoconazole
Active Ingredient(s): 20    mg/g & nbsp;   ketoconazole
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ketoconazole

Product NDC: 52125-375
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076294
Marketing Category: ANDA
Start Marketing Date: 20130612

Package Information of ketoconazole

Package NDC: 52125-375-01
Package Description: 30 g in 1 TUBE (52125-375-01)

NDC Information of ketoconazole

NDC Code 52125-375-01
Proprietary Name ketoconazole
Package Description 30 g in 1 TUBE (52125-375-01)
Product NDC 52125-375
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketoconazole
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130612
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name KETOCONAZOLE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of ketoconazole


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