NDC 70518-0761

Ibuprofen 600 mg tablet, film coated

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-320.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Granules India LimitedMedchal-Malkajgiri District, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyFeb 14, 2020 · 6 inspections

Product details

Generic drug
Ibuprofen: every company that makes it
Form
tablet, film coated, oral
Strength
600 mg
Approval
ANDA ANDA091625
On the market since
Oct 6, 2017
Package NDCs
70518-0761-0 70518-0761-1 70518-0761-2 70518-0761-3 70518-0761-4 70518-0761-5 70518-0761-6 70518-0761-7
Official label
DailyMed (National Library of Medicine), updated Jun 30, 2026

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