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  5. NDC Package Code: 0362-1098-90 Scandonest 3% Plain

NDC Package 0362-1098-90 Scandonest 3% Plain

Mepivacaine Hydrochloride Injection, Solution Subcutaneous - 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:
0362-1098-90
Package Description:
5 BLISTER PACK in 1 CARTON / 10 CARTRIDGE in 1 BLISTER PACK / 1.7 mL in 1 CARTRIDGE
Product Code:
0362-1098
Proprietary Name:
Scandonest 3% Plain
Non-Proprietary Name:
Mepivacaine Hydrochloride
Substance Name:
Mepivacaine Hydrochloride
Usage Information:
Mepivacaine is indicated for production of local anesthesia for dental procedures by infiltration or nerve block in adults and pediatric patients.
11-Digit NDC Billing Format:
00362109890
NDC to RxNorm Crosswalk:
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):
Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
MEPIVACAINE HYDROCHLORIDE 30 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA088387
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-22-2017
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 0362-1098-90?

The NDC Packaged Code 0362-1098-90 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 Scandonest 3% Plain, a human prescription drug labeled by Septodont, Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form.

Is NDC 0362-1098 included in the NDC Directory?

Yes, Scandonest 3% Plain with product code 0362-1098 is active and included in the NDC Directory. The product was first marketed by Septodont, Inc. on December 22, 2017 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 0362-1098-90?

The 11-digit format is 00362109890. 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
4-4-20362-1098-905-4-200362-1098-90