NDC 43547-325
Doxycycline Hyclate 200 mg tablet, delayed release
On the label: Solco Healthcare U.S., LLC.
Where it's 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 |
Product details
- Generic drug
- Doxycycline: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA207494
- On the market since
- Nov 28, 2016
- Package NDCs
43547-325-0643547-325-1043547-325-50- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2025
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