# HYDRALAZINE HYDROCHLORIDE

NDC: 63629-5696
Generic name: hydralazine hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070406
Marketing ended: 20260831
FDA application: ANDA086242

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-5696"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-5696
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db138daf-2d2d-4730-a621-a1bd209d5b9f