NDC 0338-9579 Sodium Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0338 - Baxter Healthcare Corporation
- 0338-9579 - Sodium Chloride
Product Packages
NDC Code 0338-9579-96
Package Description: 96 BAG in 1 CARTON / 50 mL in 1 BAG
Product Details
What is NDC 0338-9579?
What are the uses for Sodium Chloride?
Which are Sodium Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Sodium Chloride?
- RxCUI: 1807631 - sodium chloride 0.9 % in 50 ML Injection
- RxCUI: 1807631 - 50 ML sodium chloride 9 MG/ML Injection
- RxCUI: 1807631 - 50 ML NaCl 9 MG/ML Injection
- RxCUI: 1807631 - sodium chloride 0.9 % per 50 ML Injection
- RxCUI: 1807632 - sodium chloride 0.9 % in 100 ML 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".