DESONATE - 10922-828-71 - (desonide)

Alphabetical Index


Drug Information of DESONATE

Product NDC: 10922-828
Proprietary Name: DESONATE
Non Proprietary Name: desonide
Active Ingredient(s): .5    mg/g & nbsp;   desonide
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of DESONATE

Product NDC: 10922-828
Labeler Name: Intendis Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021844
Marketing Category: NDA
Start Marketing Date: 20100128

Package Information of DESONATE

Package NDC: 10922-828-71
Package Description: 1 TUBE in 1 BLISTER PACK (10922-828-71) > 3.5 g in 1 TUBE

NDC Information of DESONATE

NDC Code 10922-828-71
Proprietary Name DESONATE
Package Description 1 TUBE in 1 BLISTER PACK (10922-828-71) > 3.5 g in 1 TUBE
Product NDC 10922-828
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desonide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100128
Marketing Category Name NDA
Labeler Name Intendis Inc.
Substance Name DESONIDE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of DESONATE


General Information