NDC 54868-0235 Kenalog-40
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0235 - Kenalog-40
Product Packages
NDC Code 54868-0235-0
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON / 1 mL in 1 VIAL, SINGLE-DOSE
NDC Code 54868-0235-1
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON / 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 54868-0235-2
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 54868-0235?
What are the uses for Kenalog-40?
Which are Kenalog-40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE (UNII: 1ZK20VI6TY) (Active Moiety)
Which are Kenalog-40 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- NITROGEN (UNII: N762921K75)
What is the NDC to RxNorm Crosswalk for Kenalog-40?
- RxCUI: 1085754 - triamcinolone acetonide 40 MG/ML Injectable Suspension
- RxCUI: 1085756 - Kenalog 40 MG/ML Injectable Suspension
- RxCUI: 1085756 - triamcinolone acetonide 40 MG/ML Injectable Suspension [Kenalog]
- RxCUI: 1085756 - Kenalog-40 40 MG/ML Injectable Suspension
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".