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Bisoprolol Fumarate and Hydrochlorothiazide

NDC 42799-920 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA212678
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBISOPROLOL FUMARATE (2.5 mg/1)
HYDROCHLOROTHIAZIDE (6.25 mg/1)
Marketing started20190430
Package count3

External sources

Source: openFDA. Public-domain (CC0).