NDC 33342-033 – Pramipexole dihydrochloride

Pramipexole Dihydrochloride .5 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC33342-033

Product details

Brand name
Pramipexole dihydrochloride
Generic name
Pramipexole dihydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202164
Marketed since
September 21, 2012
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
33342-033-0630 BLISTER PACK in 1 CARTON (33342-033-06) / 1 TABLET in 1 BLISTER PACKSep 21, 2012
33342-033-1090 TABLET in 1 BOTTLE (33342-033-10)Sep 21, 2012
33342-033-12100 BLISTER PACK in 1 CARTON (33342-033-12) / 1 TABLET in 1 BLISTER PACKSep 21, 2012
33342-033-15500 TABLET in 1 BOTTLE (33342-033-15)Sep 21, 2012

Recalls mentioning this NDC

Other pramipexole dihydrochloride products