# Prazosin Hydrochloride

NDC: 68788-8742
Generic name: Prazosin Hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240923

FDA application: ANDA210971

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8742"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8742
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4449fa8-a637-4780-8e19-51cb54e1ee68