NDC 70436-201
doxycycline hyclate 200 mg per 20 mL powder, for solution
On the label: Slate Run Pharmaceuticals, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hovione Pharmascience Limited | Taipa, Macau | Makes the active ingredient | Problems found, fixed voluntarilyDec 12, 2025 · 5 inspections |
Product details
- Generic drug
- Doxycycline: every company that makes it
- Form
- powder, for solution, intravenous
- Strength
- 200 mg per 20 mL
- Approval
- ANDA ANDA217685
- On the market since
- Jul 22, 2024
- Package NDCs
70436-201-3670436-201-82- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2026
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