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  5. NDC Package Code: 60505-6260-5 Zinc Sulfate

NDC Package 60505-6260-5 Zinc Sulfate

Zinc Sulfate Injection Injection Intravenous - 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:
60505-6260-5
Package Description:
25 VIAL in 1 CARTON / 5 mL in 1 VIAL (60505-6260-0)
Product Code:
60505-6260
Proprietary Name:
Zinc Sulfate
Non-Proprietary Name:
Zinc Sulfate Injection
Substance Name:
Zinc Sulfate, Unspecified Form
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:
60505626005
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Apotex Corp
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
ZINC SULFATE, UNSPECIFIED FORM 5 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA218059
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-01-2024
Listing Expiration Date:
12-31-2026
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 60505-6260-5?

The NDC Packaged Code 60505-6260-5 is assigned to a package of 25 vial in 1 carton / 5 ml in 1 vial (60505-6260-0) of Zinc Sulfate, a human prescription drug labeled by Apotex Corp. The product's dosage form is injection and is administered via intravenous form.

Is NDC 60505-6260 included in the NDC Directory?

Yes, Zinc Sulfate with product code 60505-6260 is active and included in the NDC Directory. The product was first marketed by Apotex Corp on August 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 60505-6260-5?

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 60505-6260-5?

The 11-digit format is 60505626005. 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
5-4-160505-6260-55-4-260505-6260-05