55648-781 NDC - ENTACAPONE ()

Drug Information

Product NDC: 55648-781

Proprietary Name: Entacapone

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/30/2012

Package Information

No. Package Code Package Description Billing Unit
155648-781-021 BOTTLE in 1 CARTON (55648-781-02) / 100 TABLET, FILM COATED in 1 BOTTLE
255648-781-03500 TABLET, FILM COATED in 1 BOTTLE (55648-781-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-781The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEEntacaponeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023