Sumatriptan and Naproxen Sodium
NDC 16714-891 · NorthStar RxLLC
Packages
16714-891-01 — 9 TABLET, FILM COATED in 1 BOTTLE (16714-891-01)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
11673-764 — Naproxen Sodium, 11673-819 — Naproxen Sodium and Diphenhydramine HCL, 11673-909 — naproxen sodium, 11822-0788 — Naproxen Sodium, 11822-4170 — Naproxen Sodium, 11822-4171 — Naproxen Sodium, 11822-6040 — Naproxen Sodium, 16714-796 — Sumatriptan Succinate, 16714-797 — Sumatriptan Succinate, 16714-798 — Sumatriptan Succinate, 21130-061 — Naproxen Sodium, 21130-062 — Naproxen, 21130-180 — Naproxen Sodium, 21130-593 — Naproxen Sodium, 21130-608 — Naproxen sodium, 21130-639 — diphenhydramine hydrochloride, naproxen sodium, 21130-674 — Naproxen Sodium, 21130-690 — Naproxen Sodium, 21130-748 — Naproxen Sodium, 21130-814 — Naproxen Sodium Diphenhydramine Hydrochloride, +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