Ropinirole Hydrochloride

Product NDC

0615-7539

11-digit product format

006157539

Labeler code

0615

Product ID

0615-7539_5774cadb-5f61-47a2-95f8-cc73146016de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ropinirole Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA078881

Marketing category

ANDA

Marketing start

2011-10-27

Marketing end

0000-00-00

Substance

ROPINIROLE HYDROCHLORIDE

Active strength

2 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record