NDC 51672-5306
Fluoxetine Hydrochloride 60 mg tablet, film coated
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 60 mg
- Approval
- ANDA ANDA211477
- On the market since
- Feb 15, 2019
- Package NDCs
51672-5306-251672-5306-6- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2026
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