Lurasidone Hydrochloride
NDC 47335-579 · Sun Pharmaceutical Industries, Inc.
Packages
47335-579-13 — 500 TABLET in 1 BOTTLE (47335-579-13)
47335-579-81 — 90 TABLET in 1 BOTTLE (47335-579-81)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
43598-352 — Lurasidone hydrochloride, 43598-353 — Lurasidone hydrochloride, 43598-354 — Lurasidone hydrochloride, 43598-355 — Lurasidone Hydrochloride, 46708-494 — Lurasidone Hydrochloride, 46708-495 — Lurasidone Hydrochloride, 46708-496 — Lurasidone Hydrochloride, 46708-497 — Lurasidone Hydrochloride, 46708-498 — Lurasidone Hydrochloride, 47335-578 — Lurasidone Hydrochloride, 47335-639 — Lurasidone Hydrochloride, 47335-684 — Lurasidone Hydrochloride, 47335-685 — Lurasidone Hydrochloride, 50090-6438 — lurasidone hydrochloride, 50090-7078 — lurasidone hydrochloride, 50090-7170 — lurasidone hydrochloride, 51407-832 — Lurasidone Hydrochloride, 51407-833 — Lurasidone Hydrochloride, 51407-836 — Lurasidone Hydrochloride, 51407-837 — Lurasidone Hydrochloride, +117 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