NDC 54868-2221
Imipramine Hydrochloride 50 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-313.
Where the pills inside were 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 |
Repackaging site
- Physicians Total Care, Inc., Tulsa, Oklahoma, United States · repackages it and relabels it
Product details
- Generic drug
- Imipramine: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA090441
- On the market since
- Nov 12, 1992
- Package NDCs
54868-2221-3- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2012
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