NDC 72789-542
Doxepin Hydrochloride 25 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-174.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Doxepin: every company that makes it
- Form
- capsule, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA211603
- On the market since
- Mar 27, 2019
- Package NDCs
72789-542-30- Official label
- DailyMed (National Library of Medicine), updated Nov 4, 2026
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