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Atenolol

NDC 70518-3531 · REMEDYREPACK INC.

Generic nameAtenolol
Dosage formTABLET
RouteORAL
Active ingredient(s)ATENOLOL
Strength25 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

70518-3531-0 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-3531-0)

70518-3531-1 — 30 TABLET in 1 BLISTER PACK (70518-3531-1)

70518-3531-2 — 30 TABLET in 1 BLISTER PACK (70518-3531-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68382-024 — Atenolol, 68788-4112 — Atenolol, 68788-4156 — Atenolol and Chlorthalidone, 68788-7535 — Atenolol, 68788-7616 — Atenolol, 68788-7876 — Atenolol, 68788-8527 — Atenolol, 68788-8739 — Atenolol, 68788-8834 — Atenolol, 70518-3036 — Atenolol, 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, +124 more

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