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Pramipexole Dihydrochloride

NDC 46708-005 · Alembic Pharmaceuticals Limited

Generic namePramipexole Dihydrochloride

Dosage formTABLET

RouteORAL

Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE

Strength.5 mg/1

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

Marketing categoryANDA

Packages

46708-005-90 — 90 TABLET in 1 BOTTLE (46708-005-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-035 — Pramipexole dihydrochloride, 33342-208 — Pramipexole Dihydrochloride, 33342-209 — Pramipexole Dihydrochloride, 33342-210 — Pramipexole Dihydrochloride, 33342-211 — Pramipexole Dihydrochloride, 33342-212 — Pramipexole Dihydrochloride, 33342-213 — Pramipexole Dihydrochloride, 33342-214 — Pramipexole Dihydrochloride, 46708-003 — Pramipexole Dihydrochloride, 46708-004 — Pramipexole Dihydrochloride, 46708-006 — Pramipexole Dihydrochloride, 46708-007 — Pramipexole Dihydrochloride, 46708-574 — Pramipexole Dihydrochloride, 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, +116 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.