NDC 51655-674
Hydrochlorothiazide 12.5 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Leading Pharma, LLC's NDC 69315-155.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Leading Pharma, LLC | Fairfield, NJ, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 12.5 mg
- Approval
- ANDA ANDA040702
- On the market since
- Jan 8, 2023
- Package NDCs
51655-674-2651655-674-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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