Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
Recalls
- Oct 8, 2021 · Class II · Lupin Pharmaceuticals Inc.
Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Lots: lot H002205, exp. date 08/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Imipramine: every company that makes it
- Form
- capsule, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA090444
- On the market since
- Apr 16, 2010
- Package NDCs
68180-314-0168180-314-06- Official label
- DailyMed (National Library of Medicine), updated Jan 6, 2026
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