NDC 70518-2550
Hydrochlorothiazide 12.5 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-146.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- capsule, oral
- Strength
- 12.5 mg
- Approval
- ANDA ANDA203561
- On the market since
- Jan 20, 2020
- Package NDCs
70518-2550-070518-2550-170518-2550-270518-2550-370518-2550-4- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
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