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Pramipexole Dihydrochloride

NDC 65862-609 · Aurobindo Pharma Limited

Generic namePramipexole Dihydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE
Strength1.5 mg/1
Pharmacologic classDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
Marketing categoryANDA

Packages

65862-609-78 — 10 BLISTER PACK in 1 CARTON (65862-609-78) / 10 TABLET in 1 BLISTER PACK (65862-609-10)

65862-609-90 — 90 TABLET in 1 BOTTLE (65862-609-90)

65862-609-99 — 1000 TABLET in 1 BOTTLE (65862-609-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64380-747 — pramipexole dihydrochloride, 64380-748 — pramipexole dihydrochloride, 64380-749 — pramipexole dihydrochloride, 64380-750 — pramipexole dihydrochloride, 64380-751 — pramipexole dihydrochloride, 65862-604 — Pramipexole Dihydrochloride, 65862-605 — Pramipexole Dihydrochloride, 65862-606 — Pramipexole Dihydrochloride, 65862-607 — Pramipexole Dihydrochloride, 65862-608 — Pramipexole Dihydrochloride, 68462-330 — Pramipexole dihydrochloride, 68462-331 — Pramipexole dihydrochloride, 68462-332 — Pramipexole dihydrochloride, 68462-333 — Pramipexole dihydrochloride, 68462-334 — Pramipexole dihydrochloride, 68462-627 — Pramipexole dihydrochloride, 69680-145 — Pramipexole Dihydrochloride, 69680-146 — Pramipexole Dihydrochloride, 71034-002 — Pramipexole Dihydrochloride, 71034-003 — Pramipexole Dihydrochloride, +116 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.