NDC Package 0517-6103-25 Zinc Sulfate

Injection, Solution 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:
0517-6103-25
Package Description:
25 VIAL in 1 TRAY / 10 mL in 1 VIAL (0517-6103-01)
Product Code:
Proprietary Name:
Zinc Sulfate
Non-Proprietary Name:
Zinc Sulfate
Substance Name:
Zinc Sulfate
Usage Information:
Zinc Sulfate Injection is indicated in adult and pediatric patients as a source of zinc for parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated.
11-Digit NDC Billing Format:
00517610325
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2201521 - zinc sulfate 3 MG/ML Injectable Solution
  • RxCUI: 2201521 - ZnSO4 3 MG/ML Injectable Solution
  • RxCUI: 2201524 - zinc sulfate 5 MG/ML Injectable Solution
  • RxCUI: 2201524 - ZnSO4 5 MG/ML Injectable Solution
  • RxCUI: 2369390 - zinc sulfate 1 MG in ML Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    American Regent, Inc.
    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):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA209377
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-01-2019
    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 0517-6103-25?

    The NDC Packaged Code 0517-6103-25 is assigned to a package of 25 vial in 1 tray / 10 ml in 1 vial (0517-6103-01) of Zinc Sulfate, a human prescription drug labeled by American Regent, Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 0517-6103 included in the NDC Directory?

    Yes, Zinc Sulfate with product code 0517-6103 is active and included in the NDC Directory. The product was first marketed by American Regent, Inc. on October 01, 2019 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 NDC billing unit for package 0517-6103-25?

    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 0517-6103-25?

    The 11-digit format is 00517610325. 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
    4-4-20517-6103-255-4-200517-6103-25