NDC 85534-0025
Ondansetron 4 mg tablet, orally disintegrating
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, 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 |
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
85534-0025-085534-0025-185534-0025-2- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2026
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