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Atenolol

NDC 71205-229 · Proficient Rx LP

Generic nameAtenolol
Dosage formTABLET
RouteORAL
Active ingredient(s)ATENOLOL
Strength50 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

71205-229-30 — 30 TABLET in 1 BOTTLE (71205-229-30)

71205-229-60 — 60 TABLET in 1 BOTTLE (71205-229-60)

71205-229-90 — 90 TABLET in 1 BOTTLE (71205-229-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4099 — Atenolol, 70518-4111 — Atenolol and Chlorthalidone, 70518-4287 — Atenolol, 70710-1167 — Atenolol and Chlorthalidone, 70710-1168 — Atenolol and Chlorthalidone, 70771-1372 — Atenolol and Chlorthalidone, 70771-1373 — Atenolol and Chlorthalidone, 70954-390 — Atenolol and Chlorthalidone, 70954-391 — Atenolol and Chlorthalidone, 71205-096 — Atenolol, 71205-496 — atenolol, 71335-0912 — Atenolol, 71335-0954 — Atenolol, 71335-1264 — Atenolol, 71335-1535 — Atenolol, 71335-1616 — Atenolol, 71335-2531 — Atenolol, 71335-2774 — Atenolol, 71335-9611 — Atenolol, 71610-658 — atenolol, +124 more

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