NDC 43063-857
Ondansetron 4 mg tablet, orally disintegrating
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-390.
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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA090469
- On the market since
- Apr 12, 2010
- Package NDCs
43063-857-0243063-857-0443063-857-0543063-857-0643063-857-0843063-857-1043063-857-20- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2025
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