Pramipexole dihydrochloride

Product NDC

50090-2676

11-digit product format

500902676

Labeler code

50090

Product ID

50090-2676_7e4f08fb-4502-40c4-ac88-ae37959728ff

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pramipexole dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA202164

Marketing category

ANDA

Marketing start

2012-09-21

Marketing end

0000-00-00

Substance

PRAMIPEXOLE DIHYDROCHLORIDE

Active strength

2 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