NDC 31722-910 – Pramipexole

Pramipexole Dihydrochloride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-910

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
31722-910-05500 TABLET in 1 BOTTLE (31722-910-05)Aug 1, 2015
31722-910-101000 TABLET in 1 BOTTLE (31722-910-10)Aug 1, 2015
31722-910-9090 TABLET in 1 BOTTLE (31722-910-90)Aug 1, 2015

Other Pramipexole products