Skip to main content

Pramipexole Dihydrochloride

NDC 60687-581 · American Health Packaging

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

60687-581-21 — 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-581-21) / 1 TABLET in 1 BLISTER PACK (60687-581-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57237-183 — Pramipexole Dihydrochloride, 57237-184 — Pramipexole Dihydrochloride, 57237-185 — Pramipexole Dihydrochloride, 60429-085 — Pramipexole Dihydrochloride, 60429-086 — Pramipexole Dihydrochloride, 60429-087 — Pramipexole Dihydrochloride, 60429-088 — Pramipexole Dihydrochloride, 60429-089 — Pramipexole Dihydrochloride, 60429-090 — Pramipexole Dihydrochloride, 60687-570 — Pramipexole Dihydrochloride, 60687-592 — Pramipexole Dihydrochloride, 62332-003 — Pramipexole Dihydrochloride, 62332-004 — Pramipexole Dihydrochloride, 62332-005 — Pramipexole Dihydrochloride, 62332-006 — Pramipexole Dihydrochloride, 62332-007 — Pramipexole Dihydrochloride, 62332-154 — Pramipexole Dihydrochloride, 62332-155 — Pramipexole Dihydrochloride, 62332-156 — Pramipexole Dihydrochloride, 62332-157 — 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.