desonide - 0168-0309-60 - (desonide)

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Drug Information of desonide

Product NDC: 0168-0309
Proprietary Name: desonide
Non Proprietary Name: desonide
Active Ingredient(s): .5    mg/g & nbsp;   desonide
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of desonide

Product NDC: 0168-0309
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075751
Marketing Category: ANDA
Start Marketing Date: 20101019

Package Information of desonide

Package NDC: 0168-0309-60
Package Description: 1 TUBE in 1 CARTON (0168-0309-60) > 60 g in 1 TUBE

NDC Information of desonide

NDC Code 0168-0309-60
Proprietary Name desonide
Package Description 1 TUBE in 1 CARTON (0168-0309-60) > 60 g in 1 TUBE
Product NDC 0168-0309
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desonide
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20101019
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals 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