NDC 51655-088
Hydrochlorothiazide 25 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-361.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it | Problems found, fixed voluntarilyNov 3, 2023 · 3 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
- 25 mg
- Approval
- ANDA ANDA087059
- On the market since
- Mar 6, 2023
- Package NDCs
51655-088-2651655-088-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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