NDC 70518-3511
Ondansetron Hydrochloride 8 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-076.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA078539
- On the market since
- Sep 6, 2022
- Package NDCs
70518-3511-070518-3511-1- Official label
- DailyMed (National Library of Medicine), updated Apr 10, 2026
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