# HYDRALAZINE HYDROCHLORIDE

NDC: 23155-003
Generic name: hydralazine hydrochloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070406
Marketing ended: 20260930
FDA application: ANDA086242

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a04eefaf-ba3c-448d-8ece-4aa9ab2e3508