NDC 0517-1820
Chlorothiazide Sodium 500 mg per 18 mL injection, powder, lyophilized, for solution
On the label: American Regent, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | New Albany, OH, United States | Makes it | Problems found, fixed voluntarilyJan 29, 2026 · 5 inspections |
| American Regent, Inc. | Columbus, OH, United States | Tests it | Problems found, fixed voluntarilyMar 5, 2026 · 8 inspections |
Product details
- Generic drug
- Chlorothiazide: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 18 mL
- Approval
- ANDA ANDA202561
- On the market since
- Apr 1, 2015
- Package NDCs
0517-1820-01- Official label
- DailyMed (National Library of Medicine), updated Jun 5, 2020
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