# Prazosin Hydrochloride

NDC: 0904-7022
Generic name: Prazosin Hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20181003

FDA application: ANDA210971

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f55f4db-dab3-4e50-9f71-5595fd3ccc12