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  5. NDC Package Code: 31722-241-30 Lamotrigine

NDC Package 31722-241-30 Lamotrigine

Lamotrigine Extended-release Tablet, Film Coated, Extended Release Oral - 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:
31722-241-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
31722-241
Proprietary Name:
Lamotrigine
Non-Proprietary Name:
Lamotrigine Extended-release
Substance Name:
Lamotrigine
Usage Information:
Lamotrigine is used alone or with other medications to prevent and control seizures. It may also be used to help prevent the extreme mood swings of bipolar disorder in adults. Lamotrigine is known as an anticonvulsant or antiepileptic drug. It is thought to work by restoring the balance of certain natural substances in the brain. This drug is not approved for use in children younger than 2 years due to an increased risk of side effects (such as infections).
11-Digit NDC Billing Format:
31722024130
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1098608 - lamoTRIgine 300 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1098608 - 24 HR lamotrigine 300 MG Extended Release Oral Tablet
  • RxCUI: 1098608 - lamotrigine 300 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 1146690 - lamoTRIgine 250 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1146690 - 24 HR lamotrigine 250 MG Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Camber Pharmaceuticals Inc
    Dosage Form:
    Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • LAMOTRIGINE 50 mg/1
    • Pharmacologic Class(es):
  • Anti-epileptic Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Central Nervous System Disorganized Electrical Activity - [PE] (Physiologic Effect)
  • Dihydrofolate Reductase Inhibitors - [MoA] (Mechanism of Action)
  • Mood Stabilizer - [EPC] (Established Pharmacologic Class)
  • Organic Cation Transporter 2 Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA213949
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-09-2021
    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 31722-241-30?

    The NDC Packaged Code 31722-241-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Lamotrigine, a human prescription drug labeled by Camber Pharmaceuticals Inc. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 31722-241 included in the NDC Directory?

    Yes, Lamotrigine with product code 31722-241 is active and included in the NDC Directory. The product was first marketed by Camber Pharmaceuticals Inc on December 09, 2021 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 NDC billing unit for package 31722-241-30?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 31722-241-30?

    The 11-digit format is 31722024130. 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 5-3-2 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
    5-3-231722-241-305-4-231722-0241-30