NDC 65862-928

Sumatriptan and Naproxen Sodium 85 mg / 500 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Naproxen and Sumatriptan: every company that makes it
Form
tablet, film coated, oral
Strength
85 mg / 500 mg
Approval
ANDA ANDA207457
On the market since
Feb 15, 2018
Package NDCs
65862-928-36
Official label
DailyMed (National Library of Medicine), updated Dec 5, 2024

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