DESONATE - 50419-828-12 - (desonide)

Alphabetical Index


Drug Information of DESONATE

Product NDC: 50419-828
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: 50419-828
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021844
Marketing Category: NDA
Start Marketing Date: 20061020

Package Information of DESONATE

Package NDC: 50419-828-12
Package Description: 2 TUBE in 1 CARTON (50419-828-12) > 60 g in 1 TUBE

NDC Information of DESONATE

NDC Code 50419-828-12
Proprietary Name DESONATE
Package Description 2 TUBE in 1 CARTON (50419-828-12) > 60 g in 1 TUBE
Product NDC 50419-828
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desonide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20061020
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals 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