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  5. NDC Package Code: 70518-4278-0 Lidocaine Viscous

NDC Package 70518-4278-0 Lidocaine Viscous

Lidocaine Hydrochloride Solution Oral; Topical - 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:
70518-4278-0
Package Description:
1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE
Product Code:
70518-4278
Proprietary Name:
Lidocaine Viscous
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Lidocaine is indicated for the production of topical anesthesia of irritated or inflamed mucous membranes of the mouth and pharynx. It is also useful for reducing gagging during the taking of X-ray pictures and dental impressions.
11-Digit NDC Billing Format:
70518427800
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Remedyrepack Inc.
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • 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):
LIDOCAINE HYDROCHLORIDE 20 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA088802
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-05-2025
Listing Expiration Date:
12-31-2026
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 70518-4278-0?

The NDC Packaged Code 70518-4278-0 is assigned to a package of 1 bottle in 1 carton / 100 ml in 1 bottle of Lidocaine Viscous, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is solution and is administered via oral; topical form.

Is NDC 70518-4278 included in the NDC Directory?

Yes, Lidocaine Viscous with product code 70518-4278 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on February 05, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-4278-0?

The 11-digit format is 70518427800. 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
5-4-170518-4278-05-4-270518-4278-00