NDC Package 62756-224-88 Tiagabine Hydrochloride

Tablet, Film Coated 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:
62756-224-88
Package Description:
100 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Tiagabine Hydrochloride
Non-Proprietary Name:
Tiagabine Hydrochloride
Substance Name:
Tiagabine Hydrochloride
Usage Information:
Tiagabine hydrochloride tablets are indicated as adjunctive therapy in adults and children 12 years and older in the treatment of partial seizures.
11-Digit NDC Billing Format:
62756022488
NDC to RxNorm Crosswalk:
  • RxCUI: 1299911 - tiaGABine HCl 2 MG Oral Tablet
  • RxCUI: 1299911 - tiagabine hydrochloride 2 MG Oral Tablet
  • RxCUI: 1299917 - tiaGABine HCl 4 MG Oral Tablet
  • RxCUI: 1299917 - tiagabine hydrochloride 4 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sun Pharmaceutical Industries, 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):
    Sample Package:
    No
    FDA Application Number:
    ANDA077555
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-04-2011
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    62756-224-08100 TABLET, FILM COATED in 1 BOTTLE
    62756-224-181000 TABLET, FILM COATED in 1 BOTTLE
    62756-224-8330 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 62756-224-88?

    The NDC Packaged Code 62756-224-88 is assigned to a package of 100 tablet, film coated in 1 bottle of Tiagabine Hydrochloride, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 62756-224 included in the NDC Directory?

    Yes, Tiagabine Hydrochloride with product code 62756-224 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on November 04, 2011 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 62756-224-88?

    The 11-digit format is 62756022488. 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
    5-3-262756-224-885-4-262756-0224-88