NDC 67296-1508
Hydrochlorothiazide 25 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-133.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 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
- 25 mg
- Approval
- ANDA ANDA040780
- On the market since
- Jul 20, 2007
- Package NDCs
67296-1508-3- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2022
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