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Pramipexole Dihydrochloride

NDC 46708-576 · Alembic Pharmaceuticals Limited

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

Packages

46708-576-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-576-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-212 — Pramipexole Dihydrochloride, 33342-213 — Pramipexole Dihydrochloride, 33342-214 — Pramipexole Dihydrochloride, 46708-003 — Pramipexole Dihydrochloride, 46708-004 — Pramipexole Dihydrochloride, 46708-005 — Pramipexole Dihydrochloride, 46708-006 — Pramipexole Dihydrochloride, 46708-007 — Pramipexole Dihydrochloride, 46708-574 — Pramipexole Dihydrochloride, 46708-575 — 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, 46708-615 — Pramipexole Dihydrochloride, 50090-2455 — 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.