NDC Package 51662-1382-1 Lidocaine Hci

Injection 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:
51662-1382-1
Package Description:
1 SYRINGE in 1 CARTON / 5 mL in 1 SYRINGE
Product Code:
Proprietary Name:
Lidocaine Hci
Non-Proprietary Name:
Lidocaine Hci
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Lidocaine hydrochloride administered intravenously, is specifically indicated in the acute management of ventricular arrhythmias such as those occurring in relation to acute myocardial infarction, or during cardiac manipulation, such as cardiac surgery.
11-Digit NDC Billing Format:
51662138201
NDC to RxNorm Crosswalk:
  • RxCUI: 1012068 - lidocaine HCl 2 % in 5 ML Prefilled Syringe
  • RxCUI: 1012068 - 5 ML lidocaine hydrochloride 20 MG/ML Prefilled Syringe
  • RxCUI: 1012068 - lidocaine HCl 100 MG per 5 ML Prefilled Syringe
  • RxCUI: 1012068 - lidocaine HCl 2 % per 5 ML Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA083173
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-29-2019
    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.

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    Frequently Asked Questions

    What is NDC 51662-1382-1?

    The NDC Packaged Code 51662-1382-1 is assigned to a package of 1 syringe in 1 carton / 5 ml in 1 syringe of Lidocaine Hci, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 51662-1382 included in the NDC Directory?

    Yes, Lidocaine Hci with product code 51662-1382 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on October 29, 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 11-digit format for NDC 51662-1382-1?

    The 11-digit format is 51662138201. 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
    5-4-151662-1382-15-4-251662-1382-01