ropinirole

Product NDC

71335-0560

11-digit product format

713350560

Labeler code

71335

Product ID

71335-0560_cbc3905f-e2bc-4eaa-8166-2774d6d11390

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ropinirole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090135

Marketing category

ANDA

Marketing start

2010-02-25

Marketing end

0000-00-00

Substance

ROPINIROLE HYDROCHLORIDE

Active strength

0 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record