NDC 73380-4715 Iv Stabilizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73380 - Innate Pharma, Inc.
- 73380-4715 - Iv Stabilizer
Product Packages
NDC Code 73380-4715-9
Package Description: 1 VIAL in 1 CARTON / 1 mL in 1 VIAL
Product Details
What is NDC 73380-4715?
What are the uses for Iv Stabilizer?
Which are Iv Stabilizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOXETUMOMAB PASUDOTOX (UNII: 2NDX4B6N8F)
- MOXETUMOMAB PASUDOTOX (UNII: 2NDX4B6N8F) (Active Moiety)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H) (Active Moiety)
Which are Iv Stabilizer 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:
- GLYCINE (UNII: TE7660XO1C)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- SUCROSE (UNII: C151H8M554)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Iv Stabilizer?
- RxCUI: 2099309 - moxetumomab pasudotox-tdfk 1 MG Injection
- RxCUI: 2099314 - LUMOXITI 1 MG Injection
- RxCUI: 2099314 - moxetumomab pasudotox-tdfk 1 MG Injection [Lumoxiti]
- RxCUI: 2099314 - Lumoxiti 1 MG Injection
* 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".