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Desoximetasone

Desoximetasone Ointment USP, 0.25%

Approved
Approval ID

c8e2a37e-fdb2-4dd3-a728-60d2744d861a

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 29, 2010

Manufacturers
FDA

Physicians Total Care, Inc.

DUNS: 194123980

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 Code54868-5891
Application NumberANDA074286
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 11, 2011
FDA Product Classification

INGREDIENTS (3)

DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
COCONUT OILInactive
Code: Q9L0O73W7L
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT

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Desoximetasone - FDA Drug Approval Details