NDC 47335-330
Chlorothiazide Sodium 500 mg per 18 mL injection, powder, lyophilized, for solution
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Immacule Lifesciences Private Limited | Solan, India | Makes it and tests it | Serious problems, FDA actionSep 18, 2025 · 3 inspections, 1 with FDA action |
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
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 ANDA091546
- On the market since
- Aug 25, 2016
- Package NDCs
47335-330-40- Official label
- DailyMed (National Library of Medicine), updated Mar 21, 2025
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