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  5. NDC Package Code: 0093-5031-56 Tiagabine Hydrochloride

NDC Package 0093-5031-56 Tiagabine Hydrochloride

Tablet, Film Coated 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:
0093-5031-56
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
0093-5031
Proprietary Name:
Tiagabine Hydrochloride
Non-Proprietary Name:
Tiagabine Hydrochloride
Substance Name:
Tiagabine Hydrochloride
Usage Information:
Tiagabine HCl is indicated as adjunctive therapy in adults and children 12 years and older in the treatment of partial seizures.
11-Digit NDC Billing Format:
00093503156
NDC to RxNorm Crosswalk:
  • RxCUI: 1299903 - tiaGABine HCl 12 MG Oral Tablet
  • RxCUI: 1299903 - tiagabine hydrochloride 12 MG Oral Tablet
  • RxCUI: 1299909 - tiaGABine HCl 16 MG Oral Tablet
  • RxCUI: 1299909 - tiagabine hydrochloride 16 MG Oral Tablet
  • RxCUI: 1299911 - tiaGABine HCl 2 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Teva Pharmaceuticals Usa, Inc.
    Dosage Form:
    Tablet, Film Coated - 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.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • TIAGABINE HYDROCHLORIDE 4 mg/1
    • Pharmacologic Class(es):
  • Anti-epileptic Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Central Nervous System Disorganized Electrical Activity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA020646
    Marketing Category:
    NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
    Start Marketing Date:
    06-03-2016
    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 0093-5031-56?

    The NDC Packaged Code 0093-5031-56 is assigned to a package of 30 tablet, film coated in 1 bottle of Tiagabine Hydrochloride, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0093-5031 included in the NDC Directory?

    Yes, Tiagabine Hydrochloride with product code 0093-5031 is active and included in the NDC Directory. The product was first marketed by Teva Pharmaceuticals Usa, Inc. on June 03, 2016 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 0093-5031-56?

    The 11-digit format is 00093503156. 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
    4-4-20093-5031-565-4-200093-5031-56