NDC 70518-4457
Prazosin Hydrochloride 1 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ANI Pharmaceuticals, Inc.'s NDC 70954-019.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ANI Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Prazosin: every company that makes it
- Form
- capsule, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA210971
- On the market since
- Aug 26, 2025
- Package NDCs
70518-4457-070518-4457-1- Official label
- DailyMed (National Library of Medicine), updated Aug 26, 2026
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