NDC 67296-1803
Flomax 0.4 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Sanofi-Aventis U.S. LLC's NDC 0024-5837.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Patheon Inc. | Mississauga, Canada | Makes it, packages it and labels it | Problems found, fixed voluntarilyFeb 24, 2023 · 7 inspections |
| Patheon Puerto Rico, Inc. | Manati, PR, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 12, 2022 · 9 inspections |
| ScinoPharm Taiwan, Ltd. | Tainan, Taiwan | Makes the active ingredient | Serious problems, FDA actionJun 23, 2026 · 7 inspections, 1 with FDA action |
| Sixarp, LLC | Grand Rapids, MI, United States | Packages it and labels it | No problems foundMar 6, 2025 · 4 inspections |
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
- NDA NDA020579
- On the market since
- Apr 16, 2019
- Package NDCs
67296-1803-3- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
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