# Prazosin Hydrochloride

NDC: 63629-8750
Generic name: Prazosin Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20070222

FDA application: ANDA071745

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-8750"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-8750
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce926a30-d417-4fc1-8aa3-71405f09ec5e
