NDC Package 0187-0938-07 Tasmar

Tolcapone 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:
0187-0938-07
Package Description:
21 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Tasmar
Non-Proprietary Name:
Tolcapone
Substance Name:
Tolcapone
Usage Information:
This medication is used with other medications (levodopa/carbidopa) to treat Parkinson's disease. Tolcapone belongs to a class of drugs known as COMT inhibitors. Many people taking levodopa for Parkinson's have problems with the effects of the levodopa wearing off between scheduled doses, causing symptoms to return or worsen. Tolcapone blocks a certain natural substance (COMT enzyme) that breaks down levodopa in the body. This effect allows the levodopa to last longer in the system so that it doesn't wear off before the next dose.
11-Digit NDC Billing Format:
00187093807
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Bausch Health Us Llc
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:
NDA020697
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
07-27-2004
Listing Expiration Date:
12-31-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0187-0938-0190 TABLET, FILM COATED in 1 BOTTLE

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Frequently Asked Questions

What is NDC 0187-0938-07?

The NDC Packaged Code 0187-0938-07 is assigned to a package of 21 tablet, film coated in 1 bottle of Tasmar, a human prescription drug labeled by Bausch Health Us Llc. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 0187-0938 included in the NDC Directory?

Yes, Tasmar with product code 0187-0938 is active and included in the NDC Directory. The product was first marketed by Bausch Health Us Llc on July 27, 2004 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0187-0938-07?

The 11-digit format is 00187093807. 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
4-4-20187-0938-075-4-200187-0938-07