triamcinolone acetonide
TRIAMCINOLONE ACETONIDE OINTMENT USP, 0.025%, 0.1%
Approved
Approval ID
3f33ae63-5653-4a75-9f74-19d40ae20209
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 1, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 2
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 Code21695-503
Application NumberANDA085691
Product Classification
M
Marketing Category
C73584
G
Generic Name
triamcinolone acetonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 7, 2009
FDA Product Classification
INGREDIENTS (3)
Triamcinolone AcetonideActive
Quantity: 0.25 mg in 1 g
Code: F446C597KA
Classification: ACTIB
PetrolatumInactive
Code: 4T6H12BN9U
Classification: IACT
Light Mineral OilInactive
Code: N6K5787QVP
Classification: IACT
triamcinolone acetonide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-504
Application NumberANDA085691
Product Classification
M
Marketing Category
C73584
G
Generic Name
triamcinolone acetonide
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 7, 2009
FDA Product Classification
INGREDIENTS (3)
Triamcinolone AcetonideActive
Quantity: 1 mg in 1 g
Code: F446C597KA
Classification: ACTIB
PetrolatumInactive
Code: 4T6H12BN9U
Classification: IACT
Light Mineral OilInactive
Code: N6K5787QVP
Classification: IACT
Drug Labeling Information
SPL UNCLASSIFIED SECTION
LOINC: 42229-5Updated: 10/7/2009
Rx only