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Atenolol

NDC 68788-7616 · Preferred Pharmaceuticals, Inc.

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

Packages

68788-7616-1 — 100 TABLET in 1 BOTTLE (68788-7616-1)

68788-7616-3 — 30 TABLET in 1 BOTTLE (68788-7616-3)

68788-7616-6 — 60 TABLET in 1 BOTTLE (68788-7616-6)

68788-7616-9 — 90 TABLET in 1 BOTTLE (68788-7616-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4538 — Atenolol, 68071-4553 — Atenolol, 68071-4751 — Atenolol, 68071-5162 — Atenolol, 68382-022 — Atenolol, 68382-023 — Atenolol, 68382-024 — Atenolol, 68788-4112 — Atenolol, 68788-4156 — Atenolol and Chlorthalidone, 68788-7535 — Atenolol, 68788-7876 — Atenolol, 68788-8527 — Atenolol, 68788-8739 — Atenolol, 68788-8834 — Atenolol, 70518-3036 — Atenolol, 70518-3531 — Atenolol, 70518-4099 — Atenolol, 70518-4111 — Atenolol and Chlorthalidone, 70518-4287 — Atenolol, 70710-1167 — Atenolol and Chlorthalidone, +124 more

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