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Bisoprolol Fumarate

NDC 72578-112 · Viona Pharmaceuticals Inc

Generic nameBisoprolol Fumarate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)BISOPROLOL FUMARATE
Strength10 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

72578-112-01 — 100 TABLET, FILM COATED in 1 BOTTLE (72578-112-01)

72578-112-06 — 30 TABLET, FILM COATED in 1 BOTTLE (72578-112-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1678 — Bisoprolol fumarate, 71335-1769 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-1931 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-2178 — Bisoprolol Fumarate, 71335-2244 — Bisoprolol fumarate, 71335-2589 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-2616 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-9755 — Bisoprolol Fumarate, 72162-2177 — Bisoprolol fumarate, 72578-111 — Bisoprolol Fumarate, 72578-113 — bisoprolol fumarate and hydrochlorothiazide, 72578-114 — bisoprolol fumarate and hydrochlorothiazide, 72578-115 — bisoprolol fumarate and hydrochlorothiazide, 72789-392 — BISOPROLOL FUMARATE, 72789-395 — BISOPROLOL FUMARATE, 72888-092 — Bisoprolol Fumarate, 72888-093 — Bisoprolol Fumarate, 72888-233 — Bisoprolol Fumarate, 82638-107 — Bisoprolol Fumarate, 82638-108 — Bisoprolol Fumarate, +69 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.