Desoximetasone
Desoximetasone Ointment USP, 0.25%
Approved
Approval ID
c342beac-547b-4b0b-a39c-44a0961f924b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 31, 2020
Manufacturers
FDA
Actavis Pharma, Inc.
DUNS: 119723554
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 Code0472-0479
Application NumberANDA204965
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 31, 2020
FDA Product Classification
INGREDIENTS (3)
DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT