# Isosorbide Dinitrate

NDC: 0143-1769
Generic name: Isosorbide Dinitrate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19781201

FDA application: ANDA088088

## Active ingredients

- ISOSORBIDE DINITRATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-1769"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-1769
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0b9b320-0bf8-4342-b654-135ccb6755c2