NDC Package 63323-032-00 Sodium Acetate

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

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:
63323-032-00
Package Description:
20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)
Product Code:
Proprietary Name:
Sodium Acetate
Non-Proprietary Name:
Sodium Acetate
Substance Name:
Sodium Acetate
Usage Information:
Sodium Acetate Injection, USP (4 mEq per mL) is indicated as a source of sodium for addition to large volume intravenous fluids to prevent or correct hyponatremia in patients with restricted or no oral intake. It is also useful as an additive for preparing specific intravenous fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions.
11-Digit NDC Billing Format:
63323003200
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 312965 - sodium acetate 4 MEQ/ML Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fresenius Kabi Usa, Llc
    Dosage Form:
    Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA206687
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-30-2017
    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 63323-032-00?

    The NDC Packaged Code 63323-032-00 is assigned to a package of 20 vial, pharmacy bulk package in 1 tray / 100 ml in 1 vial, pharmacy bulk package (63323-032-04) of Sodium Acetate, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 63323-032 included in the NDC Directory?

    Yes, Sodium Acetate with product code 63323-032 is active and included in the NDC Directory. The product was first marketed by Fresenius Kabi Usa, Llc on October 30, 2017 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 63323-032-00?

    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 63323-032-00?

    The 11-digit format is 63323003200. 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
    5-3-263323-032-005-4-263323-0032-00