NDC 70518-4489
Prazosin Hydrochloride 1 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-271.
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
- Prazosin: every company that makes it
- Form
- capsule, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA213052
- On the market since
- Oct 1, 2025
- Package NDCs
70518-4489-070518-4489-1- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2026
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