NDC Package 50474-770-14 Briviact

Brivaracetam Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

50474-770-14

Package Description:

1 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK

Product Code:

50474-770

Proprietary Name:

Briviact

Non-Proprietary Name:

Brivaracetam

Substance Name:

Brivaracetam

Usage Information:

Brivaracetam is used to treat seizures (epilepsy).

11-Digit NDC Billing Format:

50474077014

NDC to RxNorm Crosswalk:

RxCUI: 1739749 - brivaracetam 50 MG per 10 ML Injection

RxCUI: 1739749 - 5 ML brivaracetam 10 MG/ML Injection

RxCUI: 1739754 - Briviact 50 MG in 5 ML Injection

RxCUI: 1739754 - 5 ML brivaracetam 10 MG/ML Injection [Briviact]

RxCUI: 1739754 - 5 ML Briviact 10 MG/ML Injection

Product Type:

Human Prescription Drug

Labeler Name:

Ucb, 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):

BRIVARACETAM 100 mg/1

Pharmacologic Class(es):

Epoxide Hydrolase Inhibitors - [MoA] (Mechanism of Action)

DEA Schedule:

Schedule V (CV) Substances

Sample Package:

FDA Application Number:

NDA205836

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

05-12-2016

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

50474 - Ucb, Inc.
- 50474-770 - Briviact
  - 50474-770-14 - 1 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK

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 Code	Package Description
50474-770-09	100 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
50474-770-66	1 BOTTLE in 1 CARTON / 60 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50474-770-14?

The NDC Packaged Code 50474-770-14 is assigned to a package of 1 blister pack in 1 carton / 14 tablet, film coated in 1 blister pack of Briviact, a human prescription drug labeled by Ucb, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 50474-770 included in the NDC Directory?

Yes, Briviact with product code 50474-770 is active and included in the NDC Directory. The product was first marketed by Ucb, Inc. on May 12, 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 50474-770-14?

The 11-digit format is 50474077014. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	50474-770-14	5-4-2	50474-0770-14

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