NDC 70518-4145
Ondansetron Hydrochloride 4 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-075.
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
- 4 mg
- Approval
- ANDA ANDA078539
- On the market since
- Jul 18, 2024
- Package NDCs
70518-4145-070518-4145-170518-4145-270518-4145-370518-4145-470518-4145-5- Official label
- DailyMed (National Library of Medicine), updated Oct 5, 2026
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