NDC 70518-4113
Hydrochlorothiazide 25 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA087059
- On the market since
- Jun 26, 2024
- Package NDCs
70518-4113-0- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2026
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