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Ketoconazole - 0093-0840-30 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 0093-0840
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: 0093-0840
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075581
Marketing Category: ANDA
Start Marketing Date: 20000427

Package Information of Ketoconazole

Package NDC: 0093-0840-30
Package Description: 30 g in 1 TUBE (0093-0840-30)

NDC Information of Ketoconazole

NDC Code 0093-0840-30
Proprietary Name Ketoconazole
Package Description 30 g in 1 TUBE (0093-0840-30)
Product NDC 0093-0840
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20000427
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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