ropinirole - 68462-255-11 - (ropinirole)

Alphabetical Index


Drug Information of ropinirole

Product NDC: 68462-255
Proprietary Name: ropinirole
Non Proprietary Name: ropinirole
Active Ingredient(s): 1    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: 68462-255
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090135
Marketing Category: ANDA
Start Marketing Date: 20100225

Package Information of ropinirole

Package NDC: 68462-255-11
Package Description: 10 BLISTER PACK in 1 CARTON (68462-255-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ropinirole

NDC Code 68462-255-11
Proprietary Name ropinirole
Package Description 10 BLISTER PACK in 1 CARTON (68462-255-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 68462-255
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ropinirole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100225
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of ropinirole


General Information