NDC 42847-850

Treximet 85 mg / 500 mg tablet, film coated

On the label: Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven.

India: 2United Kingdom: 1Singapore: 1United States: 1Mexico: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Divi's Laboratories LimitedVisakhapatnam District, IndiaMakes the active ingredient Problems found, fixed voluntarilyJul 19, 2024 · 8 inspections, 1 with FDA action
Glaxo Operations UK LtdWare, United KingdomMakes it and tests it Problems found, fixed voluntarilyDec 6, 2024 · 8 inspections
Glaxo Wellcome Manufacturing Pte. LtdJurong, SingaporeMakes the active ingredient and tests it Problems found, fixed voluntarilyOct 13, 2023 · 6 inspections
Halo Pharmaceutical IncWhippany, NJ, United StatesMakes it, tests it and packages it No problems foundDec 8, 2025 · 13 inspections
Industrias Químicas Falcón de México, S.A. de C.V. (DR. REDDY'S MEXICO)Morelos, MexicoMakes the active ingredient No problems foundAug 7, 2015 · 3 inspections, 1 with FDA action
Laxai Life Sciences Private LimitedMedchal-Malkajgiri District, IndiaMakes the active ingredient No problems foundMar 14, 2025 · 4 inspections
GlaxoSmithKline LLCZebulon, NC, United StatesTests it, packages it and labels it No problems foundFeb 20, 2026 · 9 inspections

Product details

Generic drug
Naproxen and Sumatriptan: every company that makes it
Form
tablet, film coated, oral
Strength
85 mg / 500 mg
Approval
NDA NDA021926
On the market since
Apr 25, 2008
Package NDCs
42847-850-09
Official label
DailyMed (National Library of Medicine), updated Dec 23, 2024

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