NDC 55111-398
Lansoprazole 15 mg capsule, delayed release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Recalls
- Mar 23, 2022 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications; during long term stability testing.
Lots: Lot # a) C2103093, Exp. 12/2023; b)C2103092, Exp. 12/2023. - Mar 23, 2022 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications; during long term stability testing.
Lots: Lot# C2102911, Exp. 12/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lansoprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 15 mg
- Approval
- ANDA ANDA091269
- On the market since
- Oct 15, 2010
- Package NDCs
55111-398-0155111-398-0555111-398-3055111-398-6055111-398-7955111-398-90- Official label
- DailyMed (National Library of Medicine), updated Mar 21, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?