NDC 71335-1877 – Pramipexole Dihydrochloride

Pramipexole Dihydrochloride .25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1877

Product details

Brand name
Pramipexole Dihydrochloride
Generic name
Pramipexole Dihydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202633
Marketed since
October 26, 2012
Listing expires
December 31, 2027
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
71335-1877-190 TABLET in 1 BOTTLE (71335-1877-1)May 28, 2021
71335-1877-230 TABLET in 1 BOTTLE (71335-1877-2)Dec 29, 2021
71335-1877-360 TABLET in 1 BOTTLE (71335-1877-3)Dec 29, 2021

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