NDC 82804-257
Ondansetron Hydrochloride 4 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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 |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
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 31, 2007
- Package NDCs
82804-257-1082804-257-1582804-257-30- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2026
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