NDC 65483-116 Proleukin
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 65483-116?
What are the uses for Proleukin?
Which are Proleukin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALDESLEUKIN (UNII: M89N0Q7EQR)
- ALDESLEUKIN (UNII: M89N0Q7EQR) (Active Moiety)
Which are Proleukin 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:
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Proleukin?
- RxCUI: 105648 - Proleukin 22,000,000 UNT Injection
- RxCUI: 105648 - aldesleukin 22000000 UNT Injection [Proleukin]
- RxCUI: 105648 - Proleukin 1.3 MG Injection
- RxCUI: 105648 - Proleukin 22000000 UNT Injection
- RxCUI: 307816 - aldesleukin 22,000,000 UNT Injection
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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".