Pramipexole Dihydrochloride
NDC 16714-917 · NorthStar RxLLC
Packages
16714-917-01 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-917-01)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0615-8551 — Pramipexole dihydrochloride, 0615-8552 — Pramipexole dihydrochloride, 0904-6704 — Pramipexole Dihydrochloride, 13668-091 — Pramipexole Dihydrochloride, 13668-092 — Pramipexole Dihydrochloride, 13668-093 — Pramipexole Dihydrochloride, 13668-094 — Pramipexole Dihydrochloride, 13668-095 — Pramipexole Dihydrochloride, 13668-184 — Pramipexole Dihydrochloride, 16714-916 — Pramipexole Dihydrochloride, 16714-918 — Pramipexole Dihydrochloride, 16714-919 — Pramipexole Dihydrochloride, 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, +116 more
Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels