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KETOCONAZOLE - 10147-0750-4 - (ketoconazole)

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Drug Information of KETOCONAZOLE

Product NDC: 10147-0750
Proprietary Name: KETOCONAZOLE
Non Proprietary Name: ketoconazole
Active Ingredient(s): 20    mg/mL & nbsp;   ketoconazole
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of KETOCONAZOLE

Product NDC: 10147-0750
Labeler Name: Patriot Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019927
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20050701

Package Information of KETOCONAZOLE

Package NDC: 10147-0750-4
Package Description: 120 mL in 1 BOTTLE (10147-0750-4)

NDC Information of KETOCONAZOLE

NDC Code 10147-0750-4
Proprietary Name KETOCONAZOLE
Package Description 120 mL in 1 BOTTLE (10147-0750-4)
Product NDC 10147-0750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketoconazole
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 20050701
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Patriot Pharmaceuticals, LLC
Substance Name KETOCONAZOLE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of KETOCONAZOLE


General Information