NDC 72789-238
Acetazolamide 125 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Eywa Pharma Inc's NDC 71930-008.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hibrow Healthcare Private Limited | Kanchipuram, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 30, 2026 · 1 inspection |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Acetazolamide: every company that makes it
- Form
- tablet, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA211556
- On the market since
- Jan 30, 2020
- Package NDCs
72789-238-01- Official label
- DailyMed (National Library of Medicine), updated Jan 5, 2026
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