# Prazosin Hydrochloride

NDC: 55289-536
Generic name: prazosin hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19890228

FDA application: ANDA072575

## 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:"55289-536"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-536
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5e129aa-2ee3-4c12-a327-5d5382cf2310