MedPath

Pediaderm TA

Triamcinolone Acetonide Cream USP, 0.1%

Approved
Approval ID

ccfbdc06-b18b-4291-9497-8d005bca9591

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 28, 2011

Manufacturers
FDA

Arbor Pharmaceuticals, Inc.

DUNS: 781796417

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Triamcinolone Acetonide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code24338-430
Application NumberANDA040039
Product Classification
M
Marketing Category
C73584
G
Generic Name
Triamcinolone Acetonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 28, 2011
FDA Product Classification

INGREDIENTS (1)

Triamcinolone AcetonideActive
Quantity: 1 mg in 1 g
Code: F446C597KA
Classification: ACTIB

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Pediaderm TA - FDA Drug Approval Details