# Bisoprolol Fumarate and Hydrochlorothiazide

NDC: 70771-1762
Generic name: bisoprolol fumarate and hydrochlorothiazide
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230301

FDA application: ANDA215666

## Active ingredients

- BISOPROLOL FUMARATE: 10 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:"70771-1762"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1762
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35ed3030-a9b3-4e4e-99cd-6d5c31ad22fa