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Ketoconazole - 21695-556-60 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 21695-556
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: 21695-556
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075638
Marketing Category: ANDA
Start Marketing Date: 20021218

Package Information of Ketoconazole

Package NDC: 21695-556-60
Package Description: 1 TUBE in 1 CARTON (21695-556-60) > 60 g in 1 TUBE

NDC Information of Ketoconazole

NDC Code 21695-556-60
Proprietary Name Ketoconazole
Package Description 1 TUBE in 1 CARTON (21695-556-60) > 60 g in 1 TUBE
Product NDC 21695-556
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20021218
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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