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Atenolol

NDC 68382-023 · Zydus Pharmaceuticals USA 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

68382-023-01 — 100 TABLET in 1 BOTTLE (68382-023-01)

68382-023-02 — 2000 TABLET in 1 BOTTLE (68382-023-02)

68382-023-10 — 1000 TABLET in 1 BOTTLE (68382-023-10)

68382-023-16 — 90 TABLET in 1 BOTTLE (68382-023-16)

68382-023-24 — 10000 TABLET in 1 BOTTLE (68382-023-24)

68382-023-40 — 5000 TABLET in 1 BOTTLE (68382-023-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3694 — Atenolol, 68071-3830 — Atenolol, 68071-3851 — Atenolol, 68071-4526 — Atenolol, 68071-4527 — Atenolol, 68071-4538 — Atenolol, 68071-4553 — Atenolol, 68071-4751 — Atenolol, 68071-5162 — Atenolol, 68382-022 — Atenolol, 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, +124 more

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