Desonide - 54868-5050-1 - (Desonide)

Alphabetical Index


Drug Information of Desonide

Product NDC: 54868-5050
Proprietary Name: Desonide
Non Proprietary Name: Desonide
Active Ingredient(s): .5    mg/g & nbsp;   Desonide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desonide

Product NDC: 54868-5050
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072354
Marketing Category: ANDA
Start Marketing Date: 20040517

Package Information of Desonide

Package NDC: 54868-5050-1
Package Description: 60 g in 1 BOTTLE, PLASTIC (54868-5050-1)

NDC Information of Desonide

NDC Code 54868-5050-1
Proprietary Name Desonide
Package Description 60 g in 1 BOTTLE, PLASTIC (54868-5050-1)
Product NDC 54868-5050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desonide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20040517
Marketing Category Name ANDA
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