# HydrALAZINE Hydrochloride

NDC: 71205-072
Generic name: HydrALAZINE Hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130630

FDA application: ANDA200770

## 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:"71205-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dfd60a79-2a30-41e6-b000-a144730099a8