# prazosin hydrochloride

NDC: 60760-820
Generic name: prazosin hydrochloride
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230103

FDA application: ANDA215697

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-820"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-820
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35a996a5-abba-838d-e063-6294a90a72a4