# IVABRADINE

NDC: 50742-362
Generic name: IVABRADINE
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240715

FDA application: ANDA214051

## Active ingredients

- IVABRADINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-362"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-362
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e70f883-8c01-4ac2-815d-4a6d561c711a