# Bisoprolol Fumarate and Hydrochlorothiazide

NDC: 42799-920
Generic name: Bisoprolol Fumarate and Hydrochlorothiazide
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190430

FDA application: ANDA212678

## Active ingredients

- BISOPROLOL FUMARATE: 2.5 mg/1
- HYDROCHLOROTHIAZIDE: 6.25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-920"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-920
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=295532b5-65c8-40c3-8d27-cfd334d12802