# Ivabradine

NDC: 72603-935
Generic name: Ivabradine
Labeler / Manufacturer: Northstar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250428

FDA application: ANDA213483

## Active ingredients

- IVABRADINE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-935"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-935
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5157767b-16d5-4a69-b6bd-95d360d19fda