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Ketoconazole - 54868-5071-3 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 54868-5071
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: 54868-5071
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075319
Marketing Category: ANDA
Start Marketing Date: 20040524

Package Information of Ketoconazole

Package NDC: 54868-5071-3
Package Description: 4 TABLET in 1 BOTTLE, PLASTIC (54868-5071-3)

NDC Information of Ketoconazole

NDC Code 54868-5071-3
Proprietary Name Ketoconazole
Package Description 4 TABLET in 1 BOTTLE, PLASTIC (54868-5071-3)
Product NDC 54868-5071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040524
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name KETOCONAZOLE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Ketoconazole


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