# prazosin hydrochloride

NDC: 70518-3679
Generic name: prazosin hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230312

FDA application: ANDA215697

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 2 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8606d9b8-4529-4689-8c93-7114c84c2e54