# prazosin hydrochloride

NDC: 70518-4712
Generic name: prazosin hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260730

FDA application: ANDA216727

## Active ingredients

- PRAZOSIN HYDROCHLORIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4712"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4712
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1f5ec80-a9bc-43b0-b3f9-4caaea861cb4