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Bisoprolol Fumarate

NDC 51407-646 · Golden State Medical Supply, Inc.

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

Packages

51407-646-01 — 100 TABLET in 1 BOTTLE (51407-646-01)

51407-646-30 — 30 TABLET in 1 BOTTLE (51407-646-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-617 — Bisoprolol fumarate, 46708-603 — BISOPROLOL FUMARATE, 46708-604 — BISOPROLOL FUMARATE, 50090-5905 — Bisoprolol Fumarate and Hydrochlorothiazide, 50090-6030 — Bisoprolol Fumarate and Hydrochlorothiazide, 50090-6413 — Bisoprolol Fumarate and Hydrochlorothiazide, 50090-6478 — bisoprolol fumarate and hydrochlorothiazide, 50090-7357 — Bisoprolol Fumarate and Hydrochlorothiazide, 50268-127 — Bisoprolol Fumarate, 51407-645 — Bisoprolol Fumarate, 52817-268 — Bisoprolol Fumarate, 52817-270 — Bisoprolol fumarate, 52817-271 — Bisoprolol fumarate, 59651-678 — Bisoprolol Fumarate and Hydrochlorothiazide, 59651-679 — Bisoprolol Fumarate and Hydrochlorothiazide, 59651-680 — Bisoprolol Fumarate and Hydrochlorothiazide, 60687-679 — Bisoprolol fumarate, 62332-603 — BISOPROLOL FUMARATE, 62332-604 — BISOPROLOL FUMARATE, 63187-871 — 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.