NDC 70518-4311
Loxapine 50 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Elite Laboratories, Inc.'s NDC 64850-893.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Elite Laboratories, Inc. | Northvale, NJ, United States | Makes it and labels it | Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action |
Product details
- Generic drug
- Loxapine: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA076868
- On the market since
- Mar 17, 2025
- Package NDCs
70518-4311-0- Official label
- DailyMed (National Library of Medicine), updated Sep 3, 2026
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