NDC 68462-334 – Pramipexole dihydrochloride

Pramipexole Dihydrochloride 1.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68462-334

Product details

Brand name
Pramipexole dihydrochloride
Generic name
Pramipexole dihydrochloride
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090781
Marketed since
October 8, 2010
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68462-334-05500 TABLET in 1 BOTTLE (68462-334-05)Oct 8, 2010
68462-334-1110 BLISTER PACK in 1 CARTON (68462-334-11) / 10 TABLET in 1 BLISTER PACKOct 8, 2010
68462-334-9090 TABLET in 1 BOTTLE (68462-334-90)Oct 8, 2010

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