55648-155 NDC - ROPINIROLE HYDROCHLORIDE ()

Drug Information

Product NDC: 55648-155

Proprietary Name: Ropinirole Hydrochloride

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:5/29/2008

Package Information

No. Package Code Package Description Billing Unit
155648-155-0130 TABLET, FILM COATED in 1 BOTTLE (55648-155-01)
255648-155-02100 TABLET, FILM COATED in 1 BOTTLE (55648-155-02)
355648-155-03500 TABLET, FILM COATED in 1 BOTTLE (55648-155-03)
455648-155-0410 BLISTER PACK in 1 CARTON (55648-155-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-155The 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 NAMERopinirole HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/29/2008This 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: 11/18/2019