NDC Package 70518-2109-0 Keppra XR

Levetiracetam Tablet, Film Coated, Extended Release Oral - 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:
70518-2109-0
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Keppra XR
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:
70518210900
NDC to RxNorm Crosswalk:
  • RxCUI: 807832 - levETIRAcetam 500 MG 24HR Extended Release Oral Tablet
  • RxCUI: 807832 - 24 HR levetiracetam 500 MG Extended Release Oral Tablet
  • RxCUI: 807832 - levetiracetam 500 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 807834 - KEPPRA XR 500 MG 24HR Extended Release Oral Tablet, Once-Daily
  • RxCUI: 807834 - 24 HR levetiracetam 500 MG Extended Release Oral Tablet [Keppra]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack 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):
    Sample Package:
    No
    FDA Application Number:
    NDA022285
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-23-2019
    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 70518-2109-0?

    The NDC Packaged Code 70518-2109-0 is assigned to a package of 30 tablet, film coated, extended release in 1 blister pack of Keppra XR, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 70518-2109 included in the NDC Directory?

    Yes, Keppra XR with product code 70518-2109 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on May 23, 2019 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 70518-2109-0?

    The 11-digit format is 70518210900. 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
    5-4-170518-2109-05-4-270518-2109-00