NDC 50090-4541 Venofer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4541 - Venofer
Product Packages
NDC Code 50090-4541-0
Package Description: 5 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 50090-4541?
What are the uses for Venofer?
Which are Venofer UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRON SUCROSE (UNII: FZ7NYF5N8L)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
Which are Venofer 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:
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Venofer?
- RxCUI: 1741267 - iron (as iron sucrose) 100 MG in 5 ML Injection
- RxCUI: 1741267 - 5 ML iron sucrose 20 MG/ML Injection
- RxCUI: 1741267 - ferric oxide, saccharated 100 MG per 5 ML Injection
- RxCUI: 1741267 - iron (as iron sucrose) 100 MG per 5 ML Injection
- RxCUI: 1741268 - Venofer (iron) 100 MG in 5 mL Injection
* Please review the disclaimer below.
Patient Education
Iron Sucrose Injection
Iron sucrose injection is used treat iron-deficiency anemia (a lower than normal number of red blood cells due to too little iron) in people with chronic kidney disease (damage to the kidneys which may worsen over time and may cause the kidneys to stop working). Iron sucrose injection is in a class of medications called iron replacement products. It works by replenishing iron stores so that the body can make more red blood cells.
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* 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".