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Pramipexole Dihydrochloride

NDC 16714-922 · NorthStar RxLLC

Generic namePramipexole Dihydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE
Strength4.5 mg/1
Pharmacologic classDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
Marketing categoryANDA

Packages

16714-922-01 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13668-092 — Pramipexole Dihydrochloride, 13668-093 — Pramipexole Dihydrochloride, 13668-094 — Pramipexole Dihydrochloride, 13668-095 — Pramipexole Dihydrochloride, 13668-184 — Pramipexole Dihydrochloride, 16714-916 — Pramipexole Dihydrochloride, 16714-917 — Pramipexole Dihydrochloride, 16714-918 — Pramipexole Dihydrochloride, 16714-919 — Pramipexole Dihydrochloride, 16714-920 — 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, 31722-908 — PRAMIPEXOLE, 31722-909 — PRAMIPEXOLE, +116 more

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