Sodium Chloride Injection, Solution
NDC Package 64253-202-30
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 Medefil, Inc., this product is identified by NDC 64253-202 and is authorized under FDA application NDA202832.
Identification & Billing
- RxCUI: 727820 - sodium chloride 0.9 % in 10 ML Prefilled Syringe
- RxCUI: 727820 - 10 ML sodium chloride 9 MG/ML Prefilled Syringe
- RxCUI: 727820 - 10 ML NaCl 9 MG/ML Prefilled Syringe
- RxCUI: 727820 - sodium chloride 0.9 % per 10 ML Prefilled Syringe
Clinical Specifications
- Intramuscular - Administration within a muscle.
- Intravenous - Administration within or into a vein or veins.
- Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Regulatory & Marketing
Hierarchy Structure
- 64253 - Medefil, Inc.
- 64253-202 - Sodium Chloride
- 64253-202-30 - 60 SYRINGE, PLASTIC in 1 BOX / 10 mL in 1 SYRINGE, PLASTIC
- 64253-202 - 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 64253-202-30 identifies a specific commercial package of 60 syringe, plastic in 1 box / 10 ml in 1 syringe, plastic of Sodium Chloride, a human prescription drug labeled by Medefil, Inc.. This injection, solution is formulated for intramuscular; intravenous; subcutaneous 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 Medefil, Inc. on January 13, 2012. The current certification is valid through December 31, 2027.
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 Medefil, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 64253020230. 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.