# Hydralazine Hydrochloride

NDC: 70518-2551
Generic name: Hydralazine Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200122

FDA application: ANDA040901

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2551"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2551
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=89afc8ef-27c4-489a-81de-3f8f65f6bbb8