# Hydralazine Hydrochloride

NDC: 0904-7448
Generic name: Hydralazine Hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250103

FDA application: ANDA040858

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7448"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7448
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6ccd35e-f69c-4eef-a456-905e030ae911