NDC Package 70518-2011-0 Lidocaine Hydrochloride

Injection, Solution Infiltration; Perineural - 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:
70518-2011-0
Package Description:
25 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE (70518-2011-1)
Product Code:
Proprietary Name:
Lidocaine Hydrochloride
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Lidocaine hydrochloride injection, USP is indicated for production of local or regional anesthesia by infiltration techniques, such as percutaneous injection, and by peripheral nerve block techniques such as brachial plexus and intercostal, when the accepted procedures for these techniques as described in standard textbooks are observed.
11-Digit NDC Billing Format:
70518201100
NDC to RxNorm Crosswalk:
  • RxCUI: 1010033 - lidocaine HCl 1 % Injectable Solution
  • RxCUI: 1010033 - lidocaine hydrochloride 10 MG/ML Injectable Solution
  • RxCUI: 1010033 - lidocaine hydrochloride 1 % Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    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):
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Perineural - Administration surrounding a nerve or nerves.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA207182
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-11-2019
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70518-2011-0?

    The NDC Packaged Code 70518-2011-0 is assigned to a package of 25 vial, multi-dose in 1 carton / 10 ml in 1 vial, multi-dose (70518-2011-1) of Lidocaine Hydrochloride, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is injection, solution and is administered via infiltration; perineural form.

    Is NDC 70518-2011 included in the NDC Directory?

    Yes, Lidocaine Hydrochloride with product code 70518-2011 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on April 11, 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 70518-2011-0?

    The 11-digit format is 70518201100. 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
    5-4-170518-2011-05-4-270518-2011-00