NDC Package 70518-2147-0 Lidocaine

Ointment Topical - 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:
70518-2147-0
Package Description:
1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Code:
Proprietary Name:
Lidocaine
Non-Proprietary Name:
Lidocaine
Substance Name:
Lidocaine
Usage Information:
This product is used to help reduce itching and pain from certain skin conditions (such as scrapes, minor skin irritations, insect bites). It may also be used to help relieve nerve pain after shingles (infection with herpes zoster virus). Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.
11-Digit NDC Billing Format:
70518214700
NDC to RxNorm Crosswalk:
  • RxCUI: 1543069 - lidocaine 5 % Topical Ointment
  • RxCUI: 1543069 - lidocaine 0.05 MG/MG Topical Ointment
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA207810
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-14-2019
    Listing Expiration Date:
    12-31-2024
    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 70518-2147-0?

    The NDC Packaged Code 70518-2147-0 is assigned to a package of 1 tube in 1 carton / 50 g in 1 tube of Lidocaine, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is ointment and is administered via topical form.

    Is NDC 70518-2147 included in the NDC Directory?

    Yes, Lidocaine with product code 70518-2147 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on June 14, 2019 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 11-digit format for NDC 70518-2147-0?

    The 11-digit format is 70518214700. 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
    5-4-170518-2147-05-4-270518-2147-00