# Prazosin hydrochloride

NDC: 70377-067
Generic name: Prazosin hydrochloride
Labeler / Manufacturer: Biocon Pharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230109

FDA application: ANDA213406

## 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:"70377-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70377-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82a84f69-4742-453f-96c8-532fb7df44c6