NDC Package 0362-1096-70 Lignospan Forte

Lidocaine Hydrochloride And Epinephrine Injection, Solution Submucosal - 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:
0362-1096-70
Package Description:
5 BLISTER PACK in 1 CARTON / 10 CARTRIDGE in 1 BLISTER PACK / 1.7 mL in 1 CARTRIDGE
Product Code:
Proprietary Name:
Lignospan Forte
Non-Proprietary Name:
Lidocaine Hydrochloride And Epinephrine
Substance Name:
Epinephrine Bitartrate; Lidocaine Hydrochloride
Usage Information:
LIGNOSPAN Solutions are indicated for the production of local anesthesia for dental procedures by nerve block or infiltration techniques.Only accepted procedures for these techniques as described in standard textbooks are recommended.
11-Digit NDC Billing Format:
00362109670
NDC to RxNorm Crosswalk:
  • RxCUI: 1011814 - Lignospan forte 2 % / 1:50,000 in 1.7 mL Dental Cartridge
  • RxCUI: 1011814 - 1.7 ML epinephrine 0.02 MG/ML / lidocaine hydrochloride 20 MG/ML Cartridge [Lignospan]
  • RxCUI: 1011814 - Lignospan forte 2 % / 1:50,000 1.7 ML Dental Cartridge
  • RxCUI: 1657026 - lidocaine HCl 2 % with EPINEPHrine 1:50,000 in 1.7 ML Dental Cartridge
  • RxCUI: 1657026 - 1.7 ML epinephrine 0.02 MG/ML / lidocaine hydrochloride 20 MG/ML Cartridge
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Septodont, 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):
  • Submucosal - Administration beneath the mucous membrane.
  • Sample Package:
    No
    FDA Application Number:
    ANDA088389
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-01-2017
    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 0362-1096-70?

    The NDC Packaged Code 0362-1096-70 is assigned to a package of 5 blister pack in 1 carton / 10 cartridge in 1 blister pack / 1.7 ml in 1 cartridge of Lignospan Forte, a human prescription drug labeled by Septodont, Inc.. The product's dosage form is injection, solution and is administered via submucosal form.

    Is NDC 0362-1096 included in the NDC Directory?

    Yes, Lignospan Forte with product code 0362-1096 is active and included in the NDC Directory. The product was first marketed by Septodont, Inc. on December 01, 2017 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 0362-1096-70?

    The 11-digit format is 00362109670. 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 4-4-2 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
    4-4-20362-1096-705-4-200362-1096-70