desoximetasone
Desoximetasone Ointment USP, 0.25%
Approved
Approval ID
4025ed23-a591-4754-8dbb-4da18f49a3e3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 8, 2022
Manufacturers
FDA
Padagis Israel Pharmaceuticals Ltd
DUNS: 600093611
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Desoximetasone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code45802-496
Application NumberANDA077770
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 8, 2019
FDA Product Classification
INGREDIENTS (3)
DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT