NDC Package 68382-396-01 Sodium Phenylacetate And Sodium Benzoate

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:
68382-396-01
Package Description:
1 VIAL in 1 CARTON / 50 mL in 1 VIAL
Product Code:
Proprietary Name:
Sodium Phenylacetate And Sodium Benzoate
Non-Proprietary Name:
Sodium Phenylacetate And Sodium Benzoate
Substance Name:
Sodium Benzoate; Sodium Phenylacetate
11-Digit NDC Billing Format:
68382039601
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 984118 - sodium benzoate 10 % / sodium phenylacetate 10 % in 50 ML Injection
  • RxCUI: 984118 - 50 ML sodium benzoate 100 MG/ML / sodium phenylacetate 100 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Zydus Pharmaceuticals Usa Inc.
    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.
  • Sample Package:
    No
    FDA Application Number:
    ANDA205880
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-08-2021
    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 68382-396-01?

    The NDC Packaged Code 68382-396-01 is assigned to a package of 1 vial in 1 carton / 50 ml in 1 vial of Sodium Phenylacetate And Sodium Benzoate, a human prescription drug labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 68382-396 included in the NDC Directory?

    Yes, Sodium Phenylacetate And Sodium Benzoate with product code 68382-396 is active and included in the NDC Directory. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on February 08, 2021 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 68382-396-01?

    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 68382-396-01?

    The 11-digit format is 68382039601. 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
    5-3-268382-396-015-4-268382-0396-01