desonide - 0168-0310-04 - (desonide)

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Drug Information of desonide

Product NDC: 0168-0310
Proprietary Name: desonide
Non Proprietary Name: desonide
Active Ingredient(s): .5    mg/1000mL & nbsp;   desonide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of desonide

Product NDC: 0168-0310
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075860
Marketing Category: ANDA
Start Marketing Date: 20020319

Package Information of desonide

Package NDC: 0168-0310-04
Package Description: 1 BOTTLE in 1 CARTON (0168-0310-04) > 118 mL in 1 BOTTLE

NDC Information of desonide

NDC Code 0168-0310-04
Proprietary Name desonide
Package Description 1 BOTTLE in 1 CARTON (0168-0310-04) > 118 mL in 1 BOTTLE
Product NDC 0168-0310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desonide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20020319
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name DESONIDE
Strength Number .5
Strength Unit mg/1000mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of desonide


General Information