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  5. NDC Package Code: 63323-186-20 Sodium Chloride

NDC Package 63323-186-20 Sodium Chloride

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
63323-186-20
Package Description:
25 VIAL, SINGLE-DOSE in 1 TRAY / 20 mL in 1 VIAL, SINGLE-DOSE (63323-186-03)
Product Code:
63323-186
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:
63323018620
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1807632 - sodium chloride 0.9 % in 100 ML Injection
  • RxCUI: 1807632 - 100 ML sodium chloride 9 MG/ML Injection
  • RxCUI: 1807632 - 100 ML NaCl 9 MG/ML Injection
  • RxCUI: 1807632 - sodium chloride 0.9 % per 100 ML Injection
  • RxCUI: 1807636 - sodium chloride 0.9 % in 2 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fresenius Kabi Usa, Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    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.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 9 mg/mL
  • 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)
  • 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:
    ANDA088912
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-10-2000
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63323-186-0025 VIAL, SINGLE-DOSE in 1 TRAY / 100 mL in 1 VIAL, SINGLE-DOSE
    63323-186-0225 VIAL, SINGLE-DOSE in 1 TRAY / 2 mL in 1 VIAL, SINGLE-DOSE (63323-186-04)
    63323-186-1025 VIAL, SINGLE-DOSE in 1 TRAY / 10 mL in 1 VIAL, SINGLE-DOSE (63323-186-01)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63323-186-20?

    The NDC Packaged Code 63323-186-20 is assigned to a package of 25 vial, single-dose in 1 tray / 20 ml in 1 vial, single-dose (63323-186-03) of Sodium Chloride, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 63323-186 included in the NDC Directory?

    Yes, Sodium Chloride with product code 63323-186 is active and included in the NDC Directory. The product was first marketed by Fresenius Kabi Usa, Llc on August 10, 2000 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 NDC billing unit for package 63323-186-20?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 63323-186-20?

    The 11-digit format is 63323018620. 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 5-3-2 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
    5-3-263323-186-205-4-263323-0186-20