Tridesilon Cream
Approved
Approval ID
30d60cbc-fba8-7209-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 21, 2016
Manufacturers
FDA
Encore Dermatology Inc
DUNS: 079629654
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
desonide 0.05%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69482-600
Application NumberNDA017010
Product Classification
M
Marketing Category
C73594
G
Generic Name
desonide 0.05%
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 21, 2016
FDA Product Classification
INGREDIENTS (1)
DESONIDEActive
Quantity: 0.03 g in 60 g
Code: J280872D1O
Classification: ACTIB