NDC 70518-1588
Imipramine Hydrochloride 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Leading Pharma, LLC's NDC 69315-135.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Leading Pharma, LLC | Fairfield, NJ, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections |
Product details
- Generic drug
- Imipramine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA040903
- On the market since
- Oct 25, 2018
- Package NDCs
70518-1588-0- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2026
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