NDC 67296-2220
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Northstar Rx LLC.'s NDC 72603-115.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 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, oral
- Strength
- 0.4 mg
- Approval
- ANDA ANDA202433
- On the market since
- Apr 30, 2013
- Package NDCs
67296-2220-167296-2220-267296-2220-3- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2026
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