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  5. NDC Package Code: 80705-100-30 Elepsia Xr 1000 Mg

NDC Package 80705-100-30 Elepsia Xr 1000 Mg

Levetiracetam Tablet, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
80705-100-30
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
80705-100
Proprietary Name:
Elepsia Xr 1000 Mg
Non-Proprietary Name:
Levetiracetam
Substance Name:
Levetiracetam
Usage Information:
Levetiracetam is used to treat seizures (epilepsy). It belongs to a class of drugs known as anticonvulsants. Levetiracetam may decrease the number of seizures you have.
11-Digit NDC Billing Format:
80705010030
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: 1605362 - levETIRAcetam 1000 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1605362 - 24 HR levetiracetam 1000 MG Extended Release Oral Tablet
  • RxCUI: 1605362 - levetiracetam 1000 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 1605368 - Elepsia XR 1000 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1605368 - 24 HR levetiracetam 1000 MG Extended Release Oral Tablet [Elepsia]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Tripoint Therapeutics, Llc
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • LEVETIRACETAM 1000 mg/1
    • Pharmacologic Class(es):
  • Decreased Central Nervous System Disorganized Electrical Activity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA204417
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-12-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    80705-100-021 BLISTER PACK in 1 CARTON / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    80705-100-991 BLISTER PACK in 1 CARTON / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80705-100-30?

    The NDC Packaged Code 80705-100-30 is assigned to a package of 30 tablet, extended release in 1 bottle, plastic of Elepsia Xr 1000 Mg, a human prescription drug labeled by Tripoint Therapeutics, Llc. The product's dosage form is tablet, extended release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

    Is NDC 80705-100 included in the NDC Directory?

    Yes, Elepsia Xr 1000 Mg with product code 80705-100 is active and included in the NDC Directory. The product was first marketed by Tripoint Therapeutics, Llc on February 12, 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 80705-100-30?

    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 80705-100-30?

    The 11-digit format is 80705010030. 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
    5-3-280705-100-305-4-280705-0100-30