MedPath

Desoximetasone

Desoximetasone Ointment USP, 0.25%For topical use only. Not for oral, ophthalmic or intravaginal use.Rx only

Approved
Approval ID

bcbc8163-dcf7-458f-a470-1e1a2edf2cc7

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 14, 2016

Manufacturers
FDA

GROUPE PARIMA INC

DUNS: 252437850

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 Code65179-500
Application NumberANDA204272
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateFebruary 24, 2014
FDA Product Classification

INGREDIENTS (3)

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

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