NDC 23155-009
Hydrochlorothiazide 50 mg tablet
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA085182
- On the market since
- Jan 15, 2015
- Package NDCs
23155-009-0123155-009-0523155-009-1023155-009-18- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2025
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