NDC 70934-032
Ibuprofen 800 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. 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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages 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
- Apr 4, 2017
- Package NDCs
70934-032-1570934-032-2170934-032-3070934-032-4070934-032-6070934-032-90- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2020
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