Sodium Chloride Injection, Solution
NDC Package 17271-700-07
Package Information
Sodium Chloride injection is this solution is used to supply water and salt (sodium chloride) to the body. This formulation utilizes a injection, solution delivery system. Marketed by Becton Dickinson And Company, this product is identified by NDC 17271-700 and is authorized under FDA application ANDA208122.
Identification & Billing
- RxCUI: 1807548 - sodium chloride 0.45 % in 50 ML Injection
- RxCUI: 1807548 - 50 ML sodium chloride 4.5 MG/ML Injection
- RxCUI: 1807548 - 50 ML NaCl 4.5 MG/ML Injection
- RxCUI: 1807548 - sodium chloride 0.45 % per 50 ML Injection
- RxCUI: 1807549 - sodium chloride 0.45 % in 100 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 17271 - Becton Dickinson And Company
- 17271-700 - Sodium Chloride
- 17271-700-07 - 10 BAG in 1 CASE / 1000 mL in 1 BAG
- 17271-700 - Sodium Chloride
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (17271-700). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 17271-700-07 identifies a specific commercial package of 10 bag in 1 case / 1000 ml in 1 bag of Sodium Chloride, a human prescription drug labeled by Becton Dickinson And Company. This injection, solution is formulated for intravenous use and contains sodium chloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Becton Dickinson And Company on July 23, 2018. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This solution is used to supply water and salt (sodium chloride) to the body. Sodium chloride solution may also be mixed with other medications given by injection into a vein.
How is this Becton Dickinson And Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 17271070007. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.