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Pramipexole Dihydrochloride

NDC 46708-615 · Alembic Pharmaceuticals 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

46708-615-90 — 90 TABLET in 1 BOTTLE (46708-615-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-575 — Pramipexole Dihydrochloride, 46708-576 — Pramipexole Dihydrochloride, 46708-577 — Pramipexole Dihydrochloride, 46708-578 — Pramipexole Dihydrochloride, 46708-579 — Pramipexole Dihydrochloride, 46708-580 — Pramipexole Dihydrochloride, 46708-611 — Pramipexole Dihydrochloride, 46708-612 — Pramipexole Dihydrochloride, 46708-613 — Pramipexole Dihydrochloride, 46708-614 — 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, 50228-130 — Pramipexole Dihydrochloride, 50228-131 — 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.