NDC 27241-304

Oxcarbazepine 150 mg tablet, extended release

On the label: Ajanta Pharma USA Inc..

India: 1Canada: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Jubilant Biosys LimitedMysuru, IndiaMakes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarilyDec 13, 2022 · 5 inspections, 1 with FDA action
Patheon Inc.Whitby, CanadaMakes it, packages it and labels it Problems found, fixed voluntarilyFeb 17, 2023 · 8 inspections
Alpha Laboratories Inc.Toronto, CanadaTests it No problems foundSep 24, 2025 · 5 inspections, 1 with FDA action
Amri Ssci, LLCLocation not on fileTests it Not inspected on record
AndersonBrecon Inc.Rockford, IL, United StatesPackages it and labels it No problems foundAug 19, 2026 · 11 inspections
Element Materials Technology Life Sciences Canada, Inc.Mississauga, CanadaTests it Problems found, fixed voluntarilyJan 22, 2025 · 6 inspections
Eurofins Lancaster Laboratories, LLCLancaster, PA, United StatesTests it Problems found, fixed voluntarilyAug 26, 2025 · 8 inspections
Pace Analytical Life Sciences, LLCMorrisville, NC, United StatesTests it No problems foundJul 10, 2026 · 1 inspection
Patheon Inc.Mississauga, CanadaTests it Problems found, fixed voluntarilyFeb 24, 2023 · 7 inspections
Quality Chemical LaboratoriesWilmington, NC, United StatesTests it Problems found, fixed voluntarilyNov 20, 2024 · 5 inspections
R.D. Laboratories, Inc.Washington, MO, United StatesTests it Problems found, fixed voluntarilyJan 26, 2024 · 6 inspections
Supernus Pharmaceuticals IncRockville, MD, United StatesTests it No problems foundJul 31, 2025 · 6 inspections

Product details

Generic drug
Oxcarbazepine: every company that makes it
Form
tablet, extended release
Strength
150 mg
Approval
NDA AUTHORIZED GENERIC NDA202810
On the market since
Aug 9, 2024
Package NDCs
27241-304-01
Official label
DailyMed (National Library of Medicine), updated Feb 27, 2024

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