NDC 31722-906 – Pramipexole

Pramipexole Dihydrochloride .125 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-906

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
31722-906-05500 TABLET in 1 BOTTLE (31722-906-05)Aug 1, 2015
31722-906-101000 TABLET in 1 BOTTLE (31722-906-10)Aug 1, 2015
31722-906-9090 TABLET in 1 BOTTLE (31722-906-90)Aug 1, 2015

Other Pramipexole products