REQUIP - 0007-4893-20 - (ropinirole)

Alphabetical Index


Drug Information of REQUIP

Product NDC: 0007-4893
Proprietary Name: REQUIP
Non Proprietary Name: ropinirole
Active Ingredient(s): 2    mg/1 & nbsp;   ropinirole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of REQUIP

Product NDC: 0007-4893
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020658
Marketing Category: NDA
Start Marketing Date: 19971003

Package Information of REQUIP

Package NDC: 0007-4893-20
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0007-4893-20)

NDC Information of REQUIP

NDC Code 0007-4893-20
Proprietary Name REQUIP
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0007-4893-20)
Product NDC 0007-4893
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ropinirole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19971003
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of REQUIP


General Information