NDC 71335-0584 – Pramipexole Dihydrochloride

Pramipexole Dihydrochloride .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0584

Product details

Brand name
Pramipexole Dihydrochloride
Generic name
Pramipexole Dihydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090865
Marketed since
October 8, 2010
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Pramipexole dihydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
71335-0584-190 TABLET in 1 BOTTLE (71335-0584-1)Jul 2, 2018
71335-0584-230 TABLET in 1 BOTTLE (71335-0584-2)Apr 24, 2018
71335-0584-360 TABLET in 1 BOTTLE (71335-0584-3)May 2, 2022

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