NDC 71921-182
Ibuprofen 800 mg tablet, film coated
On the label: Florida Pharmaceutical Products, LLC..
Where it's 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 |
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA071268
- On the market since
- Oct 21, 2021
- Package NDCs
71921-182-0171921-182-50- Official label
- DailyMed (National Library of Medicine), updated Aug 8, 2024
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