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Pramipexole Dihydrochloride

NDC 57237-181 · Rising Pharma Holdings, Inc.

Generic namePramipexole Dihydrochloride

Dosage formTABLET

RouteORAL

Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE

Strength.25 mg/1

Pharmacologic classDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

Marketing categoryANDA

Packages

57237-181-90 — 90 TABLET in 1 BOTTLE (57237-181-90)

57237-181-99 — 1000 TABLET in 1 BOTTLE (57237-181-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50742-334 — Pramipexole dihydrochloride, 50742-335 — Pramipexole dihydrochloride, 50742-336 — Pramipexole dihydrochloride, 50742-337 — Pramipexole dihydrochloride, 55111-611 — Pramipexole dihydrochloride, 55111-612 — Pramipexole dihydrochloride, 55111-613 — Pramipexole dihydrochloride, 55111-614 — Pramipexole dihydrochloride, 55111-615 — Pramipexole dihydrochloride, 57237-180 — Pramipexole Dihydrochloride, 57237-182 — Pramipexole Dihydrochloride, 57237-183 — Pramipexole Dihydrochloride, 57237-184 — Pramipexole Dihydrochloride, 57237-185 — Pramipexole Dihydrochloride, 60429-085 — Pramipexole Dihydrochloride, 60429-086 — Pramipexole Dihydrochloride, 60429-087 — Pramipexole Dihydrochloride, 60429-088 — Pramipexole Dihydrochloride, 60429-089 — Pramipexole Dihydrochloride, 60429-090 — 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.