NDC 67296-1850
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-160.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Tamsulosin: every company that makes it
- Form
- capsule
- Strength
- 0.4 mg
- Approval
- ANDA ANDA090931
- On the market since
- Jul 15, 2010
- Package NDCs
67296-1850-167296-1850-7- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2024
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