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  2. Wockhardt Usa Llc.
  3. NDC Product Code: 64679-711 Entacapone

NDC 64679-711 Entacapone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 64679-711?
    5. Entacapone Uses
    6. Active Ingredients UNII Codes
    7. Inactive Ingredients UNII Codes
    8. NDC to RxNorm Crosswalk
    9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64679-711
Proprietary Name:
Entacapone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wockhardt Usa Llc.
Labeler Code:
64679
Product Label ID:
01ea62f4-bfac-485a-bb4b-a9abb345749f
Start Marketing Date: [9]
08-16-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - YELLOWISH ORANGE)
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
W711
Score:
1

Product Packages

NDC Code 64679-711-01

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

NDC Code 64679-711-02

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $2.20696 per EA

NDC Code 64679-711-03

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE

NDC Code 64679-711-04

Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK

Product Details

What is NDC 64679-711?

The NDC code 64679-711 is assigned by the FDA to the product Entacapone which is product labeled by Wockhardt Usa Llc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 64679-711-01 30 tablet, film coated in 1 bottle , 64679-711-02 100 tablet, film coated in 1 bottle , 64679-711-03 500 tablet, film coated in 1 bottle , 64679-711-04 10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Entacapone?

This medication is used with other medications (levodopa/carbidopa) to treat Parkinson's disease. Entacapone 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. Entacapone blocks a certain natural substance (COMT enzyme) that breaks down the 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.

Which are Entacapone UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Entacapone Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Entacapone?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

* Please review the disclaimer below.

Patient Education

Entacapone


Entacapone is an inhibitor of catechol-O-methyltransferase (COMT). It is used in combination with levodopa and carbidopa (Sinemet) to treat the end-of-dose 'wearing-off' symptoms of Parkinson's disease. Entacapone helps the levodopa and carbidopa work better by allowing more of it to reach the brain, where it has its effects. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".