Sumatriptan and Naproxen Sodium
NDC 47335-410 · Sun Pharmaceutical Industries, Inc.
Packages
47335-410-22 — 9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22)
47335-410-83 — 30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83)
47335-410-88 — 100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
43598-495 — Naproxen sodium, 43598-768 — Sumatriptan Succinate, 44183-850 — sumatriptan succinate and naproxen sodium, 45802-490 — Naproxen Sodium, 46122-562 — Naproxen Sodium, 46122-564 — Naproxen Sodium, 46122-780 — Naproxen Sodium, 46708-656 — sumatriptan succinate, 46708-657 — sumatriptan succinate, 47335-276 — Sumatriptan Succinate, 47682-037 — Naproxen Sodium, 47682-237 — NAPROXEN SODIUM, 47682-488 — Naproxen Sodium, 47682-737 — Naproxen Sodium, 47781-153 — Naproxen Sodium, 47781-154 — Naproxen Sodium, 48201-007 — Naproxen Sodium, 49035-382 — Naproxen Sodium, 49035-748 — Naproxen Sodium, 49483-608 — NAPROXEN SODIUM, +427 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