PRAMIPEXOLE

NDC 31722-908 · Camber Pharmaceuticals, Inc.

Generic namePRAMIPEXOLE

Dosage formTABLET

RouteORAL

Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE

Strength.5 mg/1

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

Marketing categoryANDA

Packages

31722-908-05 — 500 TABLET in 1 BOTTLE (31722-908-05)

31722-908-10 — 1000 TABLET in 1 BOTTLE (31722-908-10)

31722-908-90 — 90 TABLET in 1 BOTTLE (31722-908-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-920 — Pramipexole Dihydrochloride, 16714-922 — Pramipexole Dihydrochloride, 29300-207 — pramipexole dihydrochloride, 29300-208 — pramipexole dihydrochloride, 29300-209 — pramipexole dihydrochloride, 29300-210 — pramipexole dihydrochloride, 29300-211 — pramipexole dihydrochloride, 29300-270 — pramipexole dihydrochloride, 31722-906 — PRAMIPEXOLE, 31722-907 — PRAMIPEXOLE, 31722-909 — PRAMIPEXOLE, 31722-910 — PRAMIPEXOLE, 31722-911 — PRAMIPEXOLE, 33342-031 — Pramipexole dihydrochloride, 33342-032 — Pramipexole dihydrochloride, 33342-033 — Pramipexole dihydrochloride, 33342-034 — Pramipexole dihydrochloride, 33342-035 — Pramipexole dihydrochloride, 33342-208 — Pramipexole Dihydrochloride, 33342-209 — Pramipexole Dihydrochloride, +116 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.