Pramipexole Dihydrochloride

Product NDC

68084-440

11-digit product format

680840440

Labeler code

68084

Product ID

68084-440_8c61d729-56a1-775a-e053-2a95a90aed5a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pramipexole Dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA078920

Marketing category

ANDA

Marketing start

2011-05-05

Marketing end

2020-07-31

Substance

PRAMIPEXOLE DIHYDROCHLORIDE

Active strength

0 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