NDC 70518-4363
Trazodone Hydrochloride 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-014.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Dadra, India | Makes it | Problems found, fixed voluntarilyMar 29, 2019 · 5 inspections |
Product details
- Generic drug
- Trazodone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA073137
- On the market since
- Jun 18, 2025
- Package NDCs
70518-4363-070518-4363-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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