NDC 70518-4251
Hydrochlorothiazide 12.5 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-764.
Where the pills inside were 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
- 12.5 mg
- Approval
- ANDA ANDA085182
- On the market since
- Jan 7, 2025
- Package NDCs
70518-4251-0- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
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