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
NDC Product Code52565-038
Application NumberANDA212002
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateMarch 13, 2019
Generic NameDesonide
INGREDIENTS (2)
DESONIDEActive
Quantity: 0.5 mg in 1 g
Code: J280872D1O
Classification: ACTIB
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT