Desonide
Desonide Ointment, 0.05%
Approved
Approval ID
6b2b161f-8ddf-4b16-973f-b32059f9c4d1
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 13, 2019
Manufacturers
FDA
Teligent Pharma, Inc.
DUNS: 011036910
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desonide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52565-038
Application NumberANDA212002
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 13, 2019
FDA Product Classification
INGREDIENTS (2)
DESONIDEActive
Quantity: 0.5 mg in 1 g
Code: J280872D1O
Classification: ACTIB
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT