NDC 70518-1551
Ondansetron 8 mg tablet, orally disintegrating
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-391.
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, orally disintegrating, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA090469
- On the market since
- Oct 23, 2018
- Package NDCs
70518-1551-070518-1551-170518-1551-270518-1551-3- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?