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  5. NDC Package Code: 51662-1657-1 Lidocaine Hydrochloride And Dextrose

NDC Package 51662-1657-1 Lidocaine Hydrochloride And Dextrose

Injection, Solution 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:
51662-1657-1
Package Description:
250 mL in 1 BAG
Product Code:
51662-1657
Proprietary Name:
Lidocaine Hydrochloride And Dextrose
Non-Proprietary Name:
Lidocaine Hydrochloride And Dextrose
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Lidocaine hydrochloride administered intravenously is specifically indicated in the acute management of (1) ventricular arrhythmias occurring during cardiac manipulations, such as cardiac surgery and (2) life-threatening arrhythmias which are ventricular in origin, such as occur during acute myocardial infarction.
11-Digit NDC Billing Format:
51662165701
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Hf Acquisition Co Llc, Dba Healthfirst
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):
LIDOCAINE HYDROCHLORIDE 8 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA018461
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-22-1981
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 51662-1657-1?

The NDC Packaged Code 51662-1657-1 is assigned to a package of 250 ml in 1 bag of Lidocaine Hydrochloride And Dextrose, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 51662-1657 included in the NDC Directory?

Yes, Lidocaine Hydrochloride And Dextrose with product code 51662-1657 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on April 22, 1981 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 11-digit format for NDC 51662-1657-1?

The 11-digit format is 51662165701. 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
5-4-151662-1657-15-4-251662-1657-01