Pramipexole Dihydrochloride

Product NDC

50090-1388

11-digit product format

500901388

Labeler code

50090

Product ID

50090-1388_1e043bf1-5768-4138-b05b-68f8d597bb88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pramipexole Dihydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA078920

Marketing category

ANDA

Marketing start

2010-07-10

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