1. Home
  2. Labeler Index
  3. Huvepharma Italia Srl
  4. 71886-434
  5. NDC Package Code: 71886-434-50 Vigabatrin

NDC Package 71886-434-50 Vigabatrin

Powder - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
71886-434-50
Package Description:
1 BAG in 1 DRUM / 50 kg in 1 BAG
Product Code:
71886-434
Non-Proprietary Name:
Vigabatrin
Substance Name:
Vigabatrin
Usage Information:
Vigabatrin is used to treat babies, one month to 2 years old who have a condition known as infantile spasms. Vigabatrin has also been used in combination with other medications to treat seizure disorders (epilepsy). Vigabatrin decreases the number of seizures in adults and children who have not been able to control their seizures with other treatment. Vigabatrin is an anticonvulsant. It is thought to work by stopping the breakdown of a natural calming substance (GABA) in the brain.
11-Digit NDC Billing Format:
71886043450
Product Type:
Drug For Further Processing
Labeler Name:
Huvepharma Italia Srl
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
  • VIGABATRIN 1 kg/kg
    • Sample Package:
    N/A
    Marketing Category:
    DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
    Start Marketing Date:
    01-08-1993
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 71886-434-50?

    The NDC Packaged Code 71886-434-50 is assigned to an UNFINISHED drug package of 1 bag in 1 drum / 50 kg in 1 bag of Vigabatrin, drug for further processing labeled by Huvepharma Italia Srl. The product's dosage form is powder and is administered via form.

    Is NDC 71886-434 included in the NDC Directory?

    Yes, Vigabatrin is an UNFINISHED PRODUCT with code 71886-434 that is active and included in the NDC Directory. The product was first marketed by Huvepharma Italia Srl on January 08, 1993 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 71886-434-50?

    The 11-digit format is 71886043450. 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
    5-3-271886-434-505-4-271886-0434-50