# BISOPROLOL FUMARATE

NDC: 70095-019
Generic name: BISOPROLOL FUMARATE
Labeler / Manufacturer: Sun Pharmaceutical Industries Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240310

FDA application: ANDA217617

## Active ingredients

- BISOPROLOL FUMARATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70095-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7556f457-c4d3-49d6-b383-0ade6d489091