NDC 31722-908 – Pramipexole

Pramipexole Dihydrochloride .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-908

Product details

Brand name
Pramipexole
Generic name
Pramipexole
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203855
Marketed since
August 1, 2015
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Pramipexole →

Package NDC codes (3)

Package NDCDescriptionSince
31722-908-05500 TABLET in 1 BOTTLE (31722-908-05)Aug 1, 2015
31722-908-101000 TABLET in 1 BOTTLE (31722-908-10)Aug 1, 2015
31722-908-9090 TABLET in 1 BOTTLE (31722-908-90)Aug 1, 2015

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