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Pramipexole Dihydrochloride

NDC 50228-130 · ScieGen Pharmaceuticals Inc

Generic namePramipexole Dihydrochloride

Dosage formTABLET

RouteORAL

Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE

Strength1 mg/1

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

Marketing categoryANDA

Packages

50228-130-10 — 1000 TABLET in 1 BOTTLE (50228-130-10)

50228-130-90 — 90 TABLET in 1 BOTTLE (50228-130-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-614 — Pramipexole Dihydrochloride, 46708-615 — Pramipexole Dihydrochloride, 50090-2455 — Pramipexole Dihydrochloride, 50090-3280 — Pramipexole Dihydrochloride, 50090-5036 — Pramipexole Dihydrochloride, 50090-7816 — Pramipexole Dihydrochloride, 50228-126 — Pramipexole Dihydrochloride, 50228-127 — Pramipexole Dihydrochloride, 50228-128 — Pramipexole Dihydrochloride, 50228-129 — Pramipexole Dihydrochloride, 50228-131 — Pramipexole Dihydrochloride, 50742-331 — Pramipexole dihydrochloride, 50742-332 — Pramipexole dihydrochloride, 50742-333 — Pramipexole dihydrochloride, 50742-334 — Pramipexole dihydrochloride, 50742-335 — Pramipexole dihydrochloride, 50742-336 — Pramipexole dihydrochloride, 50742-337 — Pramipexole dihydrochloride, 55111-611 — Pramipexole dihydrochloride, 55111-612 — 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.