Desoximetasone
Desoximetasone Ointment USP, 0.25%
Approved
Approval ID
ea742af6-9359-46c3-9164-ab53e8c1461e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 11, 2018
Manufacturers
FDA
Glenmark Pharmaceuticals Inc., USA
DUNS: 130597813
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 Code68462-531
Application NumberANDA202838
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 11, 2018
FDA Product Classification
INGREDIENTS (3)
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT
DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB