NDC 50268-404
Hydrochlorothiazide 12.5 mg capsule
On the label: AvPAK. It's repackaged: AvPAK rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-219.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages it and labels 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
- Dec 8, 2022
- Package NDCs
50268-404-1150268-404-15- Official label
- DailyMed (National Library of Medicine), updated Dec 8, 2022
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