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  5. NDC Package Code: 0264-9375-88 Sodium Chloride

NDC Package 0264-9375-88 Sodium Chloride

Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0264-9375-88
Package Description:
10 mL in 1 AMPULE
Product Code:
0264-9375
Proprietary Name:
Sodium Chloride
Non-Proprietary Name:
Sodium Chloride
Substance Name:
Sodium Chloride
Usage Information:
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.
11-Digit NDC Billing Format:
00264937588
NDC to RxNorm Crosswalk:
  • RxCUI: 1807637 - sodium chloride 0.9 % in 10 ML Injection
  • RxCUI: 1807637 - 10 ML sodium chloride 9 MG/ML Injection
  • RxCUI: 1807637 - 10 ML NaCl 9 MG/ML Injection
  • RxCUI: 1807637 - normal saline 10 mL Injection
  • RxCUI: 1807637 - sodium chloride 0.9 % per 10 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    B. Braun Medical Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 9 mg/mL
    • Pharmacologic Class(es):
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA019635
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-09-2016
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 0264-9375-88?

    The NDC Packaged Code 0264-9375-88 is assigned to a package of 10 ml in 1 ampule of Sodium Chloride, a human prescription drug labeled by B. Braun Medical Inc.. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 0264-9375 included in the NDC Directory?

    Yes, Sodium Chloride with product code 0264-9375 is active and included in the NDC Directory. The product was first marketed by B. Braun Medical Inc. on August 09, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0264-9375-88?

    The 11-digit format is 00264937588. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    4-4-20264-9375-885-4-200264-9375-88