NDC 70934-448
Ondansetron 8 mg tablet, orally disintegrating
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-356.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating
- Strength
- 8 mg
- Approval
- ANDA ANDA077557
- On the market since
- Sep 26, 2019
- Package NDCs
70934-448-8370934-448-95- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2020
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