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Ketoconazole - 68788-9903-1 - (Ketoconazole)

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Drug Information of Ketoconazole

Product NDC: 68788-9903
Proprietary Name: Ketoconazole
Non Proprietary Name: Ketoconazole
Active Ingredient(s): 20    mg/mL & nbsp;   Ketoconazole
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ketoconazole

Product NDC: 68788-9903
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076419
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of Ketoconazole

Package NDC: 68788-9903-1
Package Description: 118 mL in 1 BOTTLE, PLASTIC (68788-9903-1)

NDC Information of Ketoconazole

NDC Code 68788-9903-1
Proprietary Name Ketoconazole
Package Description 118 mL in 1 BOTTLE, PLASTIC (68788-9903-1)
Product NDC 68788-9903
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name SHAMPOO, SUSPENSION
Route Name TOPICAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name KETOCONAZOLE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Ketoconazole


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