# prazosin hydrochloride

NDC: 72205-276
Generic name: prazosin hydrochloride
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240917

FDA application: ANDA216727

## 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:"72205-276"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-276
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=486d4f26-60ae-4e6c-aa36-0b298a7f9aed