REQUIP

Product NDC

0007-4891

11-digit product format

000074891

Labeler code

0007

Product ID

0007-4891_1f8d4972-d7e0-4f31-a10c-6ff0936047b1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ropinirole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

GlaxoSmithKline LLC

Application

NDA020658

Marketing category

NDA

Marketing start

1997-10-10

Marketing end

2019-11-30

Substance

ROPINIROLE HYDROCHLORIDE

Active strength

1 mg/1

Pharmacologic classes

Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record