# PRAZOSIN HYDROCHLORIDE

NDC: 46708-693
Generic name: PRAZOSIN HYDROCHLORIDE
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230309

FDA application: ANDA217268

## 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:"46708-693"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-693
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fea187a3-ee8b-4463-8485-3b1de1504609