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Bisoprolol Fumarate

NDC 68788-8671 · Preferred Pharmaceuticals Inc.

Generic nameBisoprolol fumarate
Dosage formTABLET
RouteORAL
Active ingredient(s)BISOPROLOL FUMARATE
Strength5 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

68788-8671-1 — 100 TABLET in 1 BOTTLE, PLASTIC (68788-8671-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-871 — Bisoprolol fumarate, 63629-5173 — Bisoprolol fumarate, 63629-6907 — Bisoprolol fumarate, 64980-709 — Bisoprolol Fumarate, 64980-710 — Bisoprolol Fumarate, 65862-086 — Bisoprolol Fumarate, 65862-087 — Bisoprolol Fumarate, 68462-878 — Bisoprolol Fumarate and Hydrochlorothiazide, 68462-879 — Bisoprolol Fumarate and Hydrochlorothiazide, 68462-880 — Bisoprolol Fumarate and Hydrochlorothiazide, 69339-236 — Bisoprolol fumarate, 69339-237 — Bisoprolol fumarate, 70095-019 — BISOPROLOL FUMARATE, 70095-020 — BISOPROLOL FUMARATE, 70771-1726 — Bisoprolol Fumarate, 70771-1727 — Bisoprolol Fumarate, 70771-1760 — bisoprolol fumarate and hydrochlorothiazide, 70771-1761 — bisoprolol fumarate and hydrochlorothiazide, 70771-1762 — bisoprolol fumarate and hydrochlorothiazide, 70954-412 — Bisoprolol Fumarate and Hydrochlorothiazide, +69 more

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