NDC 33358-512
Ondansetron 8 mg tablet, orally disintegrating
On the label: RxChange Co.. It's repackaged: RxChange Co. 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 |
Repackaging site
- RxChange Co., Location not on file · repackages it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating
- Strength
- 8 mg
- Approval
- ANDA ANDA090469
- On the market since
- Dec 2, 2014
- Package NDCs
33358-512-30- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2014
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