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  5. NDC Package Code: 65282-1510-1 Sodium Chloride

NDC Package 65282-1510-1 Sodium Chloride

Injection, Solution Intramuscular; Intravenous; Subcutaneous - 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:
65282-1510-1
Package Description:
5 TRAY in 1 CARTON / 5 AMPULE in 1 TRAY / 10 mL in 1 AMPULE
Product Code:
65282-1510
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:
65282151001
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:
    Spectra Medical Deviecs, Llc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • 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.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 9 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    ANDA206171
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-21-2017
    Listing Expiration Date:
    12-31-2025
    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 65282-1510-1?

    The NDC Packaged Code 65282-1510-1 is assigned to a package of 5 tray in 1 carton / 5 ampule in 1 tray / 10 ml in 1 ampule of Sodium Chloride, a human prescription drug labeled by Spectra Medical Deviecs, Llc. The product's dosage form is injection, solution and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 65282-1510 included in the NDC Directory?

    Yes, Sodium Chloride with product code 65282-1510 is active and included in the NDC Directory. The product was first marketed by Spectra Medical Deviecs, Llc on July 21, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 65282-1510-1?

    The 11-digit format is 65282151001. 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 5-4-1 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
    5-4-165282-1510-15-4-265282-1510-01