KENALOG-40
KENALOG-40 INJECTION triamcinolone acetonide injectable suspension, USP
Approved
Approval ID
9c798561-a746-4176-80b3-94e5f1210271
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 29, 2010
Manufacturers
FDA
Rebel Distributors
DUNS: 118802834
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 Code21695-360
Application NumberNDA014901
Product Classification
M
Marketing Category
C73594
G
Generic Name
TRIAMCINOLONE ACETONIDE
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRA-ARTICULAR
Effective DateMarch 5, 2010
FDA Product Classification
INGREDIENTS (8)
carboxymethylcellulose sodiumInactive
Code: K679OBS311
Classification: IACT
polysorbate 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
nitrogenInactive
Code: N762921K75
Classification: IACT
sodium chlorideInactive
Code: 451W47IQ8X
Classification: IACT
benzyl alcoholInactive
Code: LKG8494WBH
Classification: IACT
sodium hydroxideInactive
Code: 55X04QC32I
Classification: IACT
triamcinolone acetonideActive
Quantity: 40 mg in 1 mL
Code: F446C597KA
Classification: ACTIB
hydrochloric acidInactive
Code: QTT17582CB
Classification: IACT