PRAMIPEXOLE

Product NDC

50090-3009

11-digit product format

500903009

Labeler code

50090

Product ID

50090-3009_0915ce06-2d76-408e-8ead-31d0bdb56ee6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PRAMIPEXOLE

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA203855

Marketing category

ANDA

Marketing start

2015-08-01

Marketing end

0000-00-00

Substance

PRAMIPEXOLE DIHYDROCHLORIDE

Active strength

1 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