# phenoxybenzamine hydrochloride

NDC: 16571-874
Generic name: phenoxybenzamine hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260826

FDA application: ANDA204551

## Active ingredients

- PHENOXYBENZAMINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-874"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-874
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d2108fa-4352-4f3f-9314-732ed8b6394c