NDC 72603-313
Lansoprazole 15 mg tablet, orally disintegrating, delayed release
On the label: Northstar Rx LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Lansoprazole: every company that makes it
- Form
- tablet, orally disintegrating, delayed release, oral
- Strength
- 15 mg
- Approval
- ANDA ANDA207167
- On the market since
- Mar 28, 2023
- Package NDCs
72603-313-0172603-313-10- Official label
- DailyMed (National Library of Medicine), updated Aug 8, 2024
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