NDC 68071-2789
Ibuprofen 800 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Florida Pharmaceutical Products, LLC.'s NDC 71921-182.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Contract Pharmacal Corp. | Hauppauge, NY, United States | Makes it | Problems found, fixed voluntarilyApr 14, 2022 · 13 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, film coated
- Strength
- 800 mg
- Approval
- ANDA ANDA071268
- On the market since
- Oct 21, 2021
- Package NDCs
68071-2789-168071-2789-268071-2789-368071-2789-5- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2022
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