# Phenoxybenzamine hydrochloride

NDC: 60219-1502
Generic name: Phenoxybenzamine hydrochloride
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20201030

FDA application: ANDA212568

## 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:"60219-1502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60219-1502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0be6a394-cd10-42fc-97cf-ad53d81d8d93