NDC 54868-5765 Lantus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5765 - Lantus
Product Packages
NDC Code 54868-5765-0
Package Description: 5 CARTRIDGE in 1 CARTON / 3 mL in 1 CARTRIDGE
Product Details
What is NDC 54868-5765?
What are the uses for Lantus?
Which are Lantus UNII Codes?
The UNII codes for the active ingredients in this product are:
- INSULIN GLARGINE (UNII: 2ZM8CX04RZ)
- INSULIN GLARGINE (UNII: 2ZM8CX04RZ) (Active Moiety)
Which are Lantus 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:
- ZINC (UNII: J41CSQ7QDS)
- METACRESOL (UNII: GGO4Y809LO)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Lantus?
- RxCUI: 285018 - Lantus 100 UNT/ML Injectable Solution
- RxCUI: 285018 - insulin glargine 100 UNT/ML Injectable Solution [Lantus]
- RxCUI: 311041 - insulin glargine 100 UNT/ML Injectable Solution
- RxCUI: 311041 - insulin analog, glargine 100 UNT/ML Injectable Solution
- RxCUI: 847230 - insulin glargine 100 UNT/ML in 3 ML Pen Injector
* Please review the disclaimer below.
[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".