Ropinirole - 60505-2869-6 - (Ropinirole)

Alphabetical Index


Drug Information of Ropinirole

Product NDC: 60505-2869
Proprietary Name: Ropinirole
Non Proprietary Name: Ropinirole
Active Ingredient(s): 3    mg/1 & nbsp;   Ropinirole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ropinirole

Product NDC: 60505-2869
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079165
Marketing Category: ANDA
Start Marketing Date: 20130329

Package Information of Ropinirole

Package NDC: 60505-2869-6
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (60505-2869-6)

NDC Information of Ropinirole

NDC Code 60505-2869-6
Proprietary Name Ropinirole
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (60505-2869-6)
Product NDC 60505-2869
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130329
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Ropinirole


General Information