NDC 70518-2052
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-598.
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 |
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, 2019
- Package NDCs
70518-2052-070518-2052-170518-2052-270518-2052-370518-2052-470518-2052-570518-2052-6- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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