NDC 76420-818
Rabeprazole Sodium 20 mg tablet, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. 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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, 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
76420-818-3076420-818-6076420-818-90- Official label
- DailyMed (National Library of Medicine), updated Feb 14, 2026
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