NDC 54868-6146 Norditropin
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Product Details
What is NDC 54868-6146?
What are the uses for Norditropin?
Which are Norditropin UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
Which are Norditropin 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:
- HISTIDINE (UNII: 4QD397987E)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- MANNITOL (UNII: 3OWL53L36A)
- PHENOL (UNII: 339NCG44TV)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Norditropin?
- RxCUI: 1736262 - somatropin 5 MG in 1.5 ML Pen Injector
- RxCUI: 1736262 - 1.5 ML somatropin 3.33 MG/ML Pen Injector
- RxCUI: 1736262 - somatropin 5 MG per 1.5 ML Pen Injector
- RxCUI: 847247 - Norditropin 5 MG in 1.5 ML Pen Injector
- RxCUI: 847247 - 1.5 ML somatropin 3.33 MG/ML Pen Injector [Norditropin]
* 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".