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Ketoconazole - 49999-301-90 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 49999-301
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: 49999-301
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075273
Marketing Category: ANDA
Start Marketing Date: 19990615

Package Information of Ketoconazole

Package NDC: 49999-301-90
Package Description: 90 TABLET in 1 BOTTLE (49999-301-90)

NDC Information of Ketoconazole

NDC Code 49999-301-90
Proprietary Name Ketoconazole
Package Description 90 TABLET in 1 BOTTLE (49999-301-90)
Product NDC 49999-301
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 Lake Erie Medical DBA Quality Care Products LLC
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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