Zinc Chloride Injection
NDC Package 51754-0102-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Zinc Chloride injection is uSP, 1 mg/mL is indicated for use as a supplement to intravenous solutions given for TPN. This formulation utilizes a injection delivery system. Marketed by Exela Pharma Sciences,llc, this product is identified by NDC 51754-0102 and is authorized under FDA application ANDA212007.

Identification & Billing

NDC Package Code
51754-0102-4
Package Description
25 VIAL in 1 CARTON / 10 mL in 1 VIAL
Product Code
51754-0102
11-Digit Billing Format
51754010204
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Zinc Chloride
Non-Proprietary Name
Zinc Chloride
Substance Name
Zinc Chloride
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
ZINC CHLORIDE 1 mg/mL
Pharmacologic Class
Usage Information
Zinc Chloride Injection, USP, 1 mg/mL is indicated for use as a supplement to intravenous solutions given for TPN. Administration helps to maintain zinc serum levels and to prevent depletion of endogenous stores, and subsequent deficiency symptoms.

Regulatory & Marketing

Labeler Name
Exela Pharma Sciences,llc
Product Type
Human Prescription Drug
FDA Application #
ANDA212007
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
08-27-2021
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51754-0102-4 identifies a specific commercial package of 25 vial in 1 carton / 10 ml in 1 vial of Zinc Chloride, a human prescription drug labeled by Exela Pharma Sciences,llc. This injection is formulated for intravenous use and contains zinc chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Exela Pharma Sciences,llc on August 27, 2021. The current certification is valid through December 31, 2026.

How is this Exela Pharma Sciences,llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51754010204. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
51754-0102-4
11-Digit CMS (5-4-2)
51754-0102-04

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.