# Prazosin Hydrochloride

NDC: 0093-4067
Generic name: Prazosin Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-4067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-4067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7293cef3-ef9e-40dc-9995-875ef047f693