NDC Package 51754-0102-4 Zinc Chloride

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

Package Information
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:

51754-0102-4

Package Description:

25 VIAL in 1 CARTON / 10 mL in 1 VIAL

Product Code:

51754-0102

Proprietary Name:

Zinc Chloride

Non-Proprietary Name:

Zinc Chloride

Substance Name:

Zinc Chloride

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.

11-Digit NDC Billing Format:

51754010204

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

RxCUI: 237508 - zinc 10 MG in 10 ML Injection

RxCUI: 237508 - 10 ML zinc chloride 1 MG/ML Injection

RxCUI: 237508 - zinc (as zinc chloride) 10 MG per 10 ML Injection

Product Type:

Human Prescription Drug

Labeler Name:

Exela Pharma Sciences,llc

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 CHLORIDE 1 mg/mL

Pharmacologic Class(es):

Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)

Decreased Copper Ion Absorption - [PE] (Physiologic Effect)

Sample Package:

FDA Application Number:

ANDA212007

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

08-27-2021

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

51754 - Exela Pharma Sciences,llc
- 51754-0102 - Zinc Chloride
  - 51754-0102-4 - 25 VIAL in 1 CARTON / 10 mL in 1 VIAL

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 51754-0102-4?

The NDC Packaged Code 51754-0102-4 is assigned to a 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. The product's dosage form is injection and is administered via intravenous form.

Is NDC 51754-0102 included in the NDC Directory?

Yes, Zinc Chloride with product code 51754-0102 is active and included in the NDC Directory. The product was first marketed by Exela Pharma Sciences,llc on August 27, 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 51754-0102-4?

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 51754-0102-4?

The 11-digit format is 51754010204. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	51754-0102-4	5-4-2	51754-0102-04

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