NDC 69367-209
Acetazolamide 500 mg capsule, extended release
On the label: Westminster Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it, packages it and labels it | Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action |
Product details
- Generic drug
- Acetazolamide: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA090779
- On the market since
- Apr 20, 2023
- Package NDCs
69367-209-01- Official label
- DailyMed (National Library of Medicine), updated Feb 17, 2026
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