Desonide - 54868-3284-1 - (Desonide)

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Drug Information of Desonide

Product NDC: 54868-3284
Proprietary Name: Desonide
Non Proprietary Name: Desonide
Active Ingredient(s): .5    mg/g & nbsp;   Desonide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Desonide

Product NDC: 54868-3284
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017010
Marketing Category: NDA
Start Marketing Date: 20060411

Package Information of Desonide

Package NDC: 54868-3284-1
Package Description: 1 TUBE in 1 CARTON (54868-3284-1) > 15 g in 1 TUBE

NDC Information of Desonide

NDC Code 54868-3284-1
Proprietary Name Desonide
Package Description 1 TUBE in 1 CARTON (54868-3284-1) > 15 g in 1 TUBE
Product NDC 54868-3284
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desonide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20060411
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name DESONIDE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Desonide


General Information