NDC 67296-1487
Hydrochlorothiazide 50 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-398.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Generics Bidco II LLC d/b/a Prinston Laboratories | Charlotte, NC, United States | Makes it | Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 50 mg
- Approval
- ANDA ANDA040412
- On the market since
- Mar 29, 2002
- Package NDCs
67296-1487-3- Official label
- DailyMed (National Library of Medicine), updated Aug 8, 2024
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