NDC 67046-0394
Doxepin hydrochloride 50 mg capsule
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-169.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Doxepin: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA212624
- On the market since
- Jun 16, 2026
- Package NDCs
67046-0394-3- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2026
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