NDC Package 69102-108-01 Roweepra

Levetiracetam Tablet 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:
69102-108-01
Package Description:
120 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Roweepra
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:
69102010801
NDC to RxNorm Crosswalk:
  • RxCUI: 1875868 - Roweepra 250 MG Oral Tablet
  • RxCUI: 1875868 - levetiracetam 250 MG Oral Tablet [Roweepra]
  • RxCUI: 311288 - levETIRAcetam 250 MG Oral Tablet
  • RxCUI: 311288 - levetiracetam 250 MG Oral Tablet
  • RxCUI: 311289 - levETIRAcetam 500 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Owp Pharmaceuticals, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA078858
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-28-2020
    Listing Expiration Date:
    12-31-2024
    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 69102-108-01?

    The NDC Packaged Code 69102-108-01 is assigned to a package of 120 tablet in 1 bottle of Roweepra, a human prescription drug labeled by Owp Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 69102-108 included in the NDC Directory?

    Yes, Roweepra with product code 69102-108 is active and included in the NDC Directory. The product was first marketed by Owp Pharmaceuticals, Inc. on October 28, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69102-108-01?

    The 11-digit format is 69102010801. 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
    5-3-269102-108-015-4-269102-0108-01