NDC 70518-4245
Ondansetron 8 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-160.
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
- Dec 20, 2024
- Package NDCs
70518-4245-0- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2026
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