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Triamcinolone acetonide

TRIAMCINOLONE 5-ASCENT

Approved
Approval ID

dca8a049-307d-45e4-bcf8-988ca7a3c942

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 12, 2016

Manufacturers
FDA

Liberty Pharmaceuticals, Inc.

DUNS: 012568840

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 Code0440-0318
Application NumberANDA088042
Product Classification
M
Marketing Category
C73584
G
Generic Name
Triamcinolone acetonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 12, 2016
FDA Product Classification

INGREDIENTS (8)

TRIAMCINOLONE ACETONIDEActive
Quantity: 5 mg in 1 g
Code: F446C597KA
Classification: ACTIB
MINERAL OILInactive
Code: T5L8T28FGP
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
SORBIC ACIDInactive
Code: X045WJ989B
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT
CETYL PALMITATEInactive
Code: 5ZA2S6B08X
Classification: IACT
POTASSIUM SORBATEInactive
Code: 1VPU26JZZ4
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT

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Triamcinolone acetonide - FDA Drug Approval Details