NDC 50436-0321
Ibuprofen 800 mg tablet, film coated
On the label: Unit Dose Services. It's repackaged: Unit Dose Services rebottles it from Ascend Laboratories, LLC's NDC 67877-321.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granules India Limited | Medchal-Malkajgiri District, India | Makes it | Problems found, fixed voluntarilyFeb 14, 2020 · 6 inspections |
Repackaging site
- Unit Dose Services, Location not on file · repackages it and relabels it
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, film coated
- Strength
- 800 mg
- Approval
- ANDA ANDA091625
- On the market since
- Dec 21, 2015
- Package NDCs
50436-0321-150436-0321-250436-0321-350436-0321-450436-0321-550436-0321-6- Official label
- DailyMed (National Library of Medicine), updated Aug 24, 2021
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