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Clobetasol Propionate - 68788-9802-3 - (Clobetasol Propionate)

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Drug Information of Clobetasol Propionate

Product NDC: 68788-9802
Proprietary Name: Clobetasol Propionate
Non Proprietary Name: Clobetasol Propionate
Active Ingredient(s): .5    mg/g & nbsp;   Clobetasol Propionate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Clobetasol Propionate

Product NDC: 68788-9802
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074248
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Clobetasol Propionate

Package NDC: 68788-9802-3
Package Description: 30 g in 1 TUBE (68788-9802-3)

NDC Information of Clobetasol Propionate

NDC Code 68788-9802-3
Proprietary Name Clobetasol Propionate
Package Description 30 g in 1 TUBE (68788-9802-3)
Product NDC 68788-9802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clobetasol Propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Clobetasol Propionate


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