REQUIP - 0007-4887-13 - (ropinirole hydrochloride)

Alphabetical Index


Drug Information of REQUIP

Product NDC: 0007-4887
Proprietary Name: REQUIP
Non Proprietary Name: ropinirole hydrochloride
Active Ingredient(s): 4    mg/1 & nbsp;   ropinirole hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of REQUIP

Product NDC: 0007-4887
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022008
Marketing Category: NDA
Start Marketing Date: 20080630

Package Information of REQUIP

Package NDC: 0007-4887-13
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0007-4887-13)

NDC Information of REQUIP

NDC Code 0007-4887-13
Proprietary Name REQUIP
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0007-4887-13)
Product NDC 0007-4887
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ropinirole hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080630
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of REQUIP


General Information