NDC 70518-3767
Doxepin hydrochloride 50 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
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, 2023
- Package NDCs
70518-3767-0- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2026
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