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Ketoconazole - 51672-4026-9 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 51672-4026
Proprietary Name: Ketoconazole
Non Proprietary Name: Ketoconazole
Active Ingredient(s): 200    mg/1 & nbsp;   Ketoconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ketoconazole

Product NDC: 51672-4026
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075319
Marketing Category: ANDA
Start Marketing Date: 19990615

Package Information of Ketoconazole

Package NDC: 51672-4026-9
Package Description: 5 BLISTER PACK in 1 BOX (51672-4026-9) > 10 TABLET in 1 BLISTER PACK

NDC Information of Ketoconazole

NDC Code 51672-4026-9
Proprietary Name Ketoconazole
Package Description 5 BLISTER PACK in 1 BOX (51672-4026-9) > 10 TABLET in 1 BLISTER PACK
Product NDC 51672-4026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990615
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name KETOCONAZOLE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Ketoconazole


General Information