# isosorbide dinitrate and hydralazine hydrochloride

NDC: 72319-012
Generic name: isosorbide dinitrate and hydralazine hydrochloride
Labeler / Manufacturer: i3 Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240207

FDA application: ANDA215988

## Active ingredients

- HYDRALAZINE HYDROCHLORIDE: 37.5 mg/1
- ISOSORBIDE DINITRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72319-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72319-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cacf1a7c-0388-09ee-e053-2995a90a10cf
