NDC 76420-523
prazosin hydrochloride 1 mg capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Lifestar Pharma LLC.'s NDC 70756-429.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 2 inspections |
Product details
- Generic drug
- Prazosin: every company that makes it
- Form
- capsule, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA215697
- On the market since
- Jan 3, 2023
- Package NDCs
76420-523-0176420-523-1076420-523-2076420-523-3076420-523-6076420-523-90- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2025
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