NDC 69668-515
Doxycycline Hyclate 150 mg tablet, delayed release
On the label: Sonoma Pharmaceuticals, Inc.. It's repackaged: Sonoma Pharmaceuticals, Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-324.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zhejiang Huahai Pharmaceutical Co., Ltd. | Linhai, China | Makes it | Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Doxycycline: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA207494
- On the market since
- Nov 28, 2016
- Package NDCs
69668-515-30- Official label
- DailyMed (National Library of Medicine), updated May 23, 2018
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