NDC 85509-1443
Rabeprazole Sodium 20 mg tablet, delayed release
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Ascend Laboratories, LLC's NDC 67877-443.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Rabeprazole: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208644
- On the market since
- Apr 27, 2018
- Package NDCs
85509-1443-385509-1443-685509-1443-9- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2025
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