Ropinirole

Product NDC

60505-2870

11-digit product format

605052870

Labeler code

60505

Product ID

60505-2870_e54a4119-e45f-82c8-b676-91125578d7d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ropinirole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Apotex Corp.

Application

ANDA079165

Marketing category

ANDA

Marketing start

2013-03-29

Marketing end

0000-00-00

Substance

ROPINIROLE HYDROCHLORIDE

Active strength

4 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