# Prazosin Hydrochloride

NDC: 43063-248
Generic name: prazosin hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19890228

FDA application: ANDA072575

## 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:"43063-248"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-248
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5d7dff44-84b1-4044-bc5a-c76ea11dd5a3