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Pramipexole dihydrochloride

NDC 50742-331 · Ingenus Pharmaceuticals, LLC

Generic namePramipexole dihydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE
Strength.375 mg/1
Pharmacologic classDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
Marketing categoryANDA

Packages

50742-331-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-331-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 50228-130 — Pramipexole Dihydrochloride, 50228-131 — 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, 55111-613 — Pramipexole dihydrochloride, 55111-614 — 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.