# Hydralazine Hydrochloride

NDC: 72162-1537
Generic name: Hydralazine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170526

FDA application: ANDA205236

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1537"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1537
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d5b0165e-9823-470a-8ed0-5c4c8722369d