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BISOPROLOL FUMARATE

NDC 70095-020 · Sun Pharmaceutical Industries Limited

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

Packages

70095-020-01 — 30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-020-01)

70095-020-02 — 100 TABLET, FILM COATED in 1 BOTTLE (70095-020-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68788-8671 — Bisoprolol fumarate, 69339-236 — Bisoprolol fumarate, 69339-237 — Bisoprolol fumarate, 70095-019 — 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, 70954-413 — Bisoprolol Fumarate and Hydrochlorothiazide, 70954-414 — Bisoprolol Fumarate and Hydrochlorothiazide, 70954-455 — Bisoprolol Fumarate, 70954-456 — 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.