ropinirole hydrochloride

Product NDC

55700-673

11-digit product format

557000673

Labeler code

55700

Product ID

55700-673_f5dd1e23-b2af-4dc1-87c9-00ddc80d2ae4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ropinirole hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA078110

Marketing category

ANDA

Marketing start

2018-08-31

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