NDC 76420-621
Lansoprazole 30 mg capsule, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-275.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Lansoprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA207394
- On the market since
- Jan 20, 2019
- Package NDCs
76420-621-3076420-621-6076420-621-90- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
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