Ropinirole - 13811-643-11 - (Ropinirole)

Alphabetical Index


Drug Information of Ropinirole

Product NDC: 13811-643
Proprietary Name: Ropinirole
Non Proprietary Name: Ropinirole
Active Ingredient(s): 12    mg/1 & nbsp;   Ropinirole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ropinirole

Product NDC: 13811-643
Labeler Name: Trigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202786
Marketing Category: ANDA
Start Marketing Date: 20130615

Package Information of Ropinirole

Package NDC: 13811-643-11
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (13811-643-11)

NDC Information of Ropinirole

NDC Code 13811-643-11
Proprietary Name Ropinirole
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (13811-643-11)
Product NDC 13811-643
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130615
Marketing Category Name ANDA
Labeler Name Trigen Laboratories, Inc.
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 12
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Ropinirole


General Information