NDC 68180-313
Imipramine Hydrochloride 50 mg tablet, film coated
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Imipramine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA090441
- On the market since
- Dec 21, 2010
- Package NDCs
68180-313-0168180-313-02- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2023
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