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PRUCALOPRIDE

NDC 0781-8158 · Sandoz Inc.

Generic namePRUCALOPRIDE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)PRUCALOPRIDE SUCCINATE
Strength1 mg/1
Pharmacologic classSerotonin 4 Receptor Agonists [MoA], Serotonin-4 Receptor Agonist [EPC]
Marketing categoryANDA

Packages

0781-8158-31 — 30 TABLET, FILM COATED in 1 BOTTLE (0781-8158-31)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0749 — Prucalopride, 0054-0750 — Prucalopride, 0781-8159 — PRUCALOPRIDE, 31722-391 — PRUCALOPRIDE, 31722-392 — PRUCALOPRIDE, 46708-077 — PRUCALOPRIDE, 46708-078 — PRUCALOPRIDE, 54092-546 — PRUCALOPRIDE, 54092-547 — PRUCALOPRIDE, 60505-4806 — Prucalopride, 60505-4807 — Prucalopride, 62332-077 — PRUCALOPRIDE, 62332-078 — PRUCALOPRIDE, 69097-218 — Prucalopride, 69097-219 — Prucalopride, 69238-2698 — Prucalopride, 69238-2699 — Prucalopride, 70069-821 — Prucalopride succinate, 70069-822 — Prucalopride succinate, 70748-389 — Prucalopride, +13 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