# prazosin hydrochloride

NDC: 76420-526
Generic name: prazosin hydrochloride
Labeler / Manufacturer: ASCLEMED USA INC.
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: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-526"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-526
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b66d105b-be78-4e54-9c01-b38e36ad74de