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Atenolol

NDC 65841-022 · Zydus Lifesciences Limited

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

Packages

65841-022-01 — 100 TABLET in 1 BOTTLE (65841-022-01)

65841-022-10 — 1000 TABLET in 1 BOTTLE (65841-022-10)

65841-022-16 — 90 TABLET in 1 BOTTLE (65841-022-16)

65841-022-24 — 10000 TABLET in 1 BOTTLE (65841-022-24)

65841-022-40 — 5000 TABLET in 1 BOTTLE (65841-022-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60429-027 — atenolol, 60687-605 — Atenolol, 60760-437 — Atenolol, 60760-642 — Atenolol, 60760-643 — Atenolol, 63187-537 — Atenolol, 63187-710 — Atenolol, 64980-437 — Atenolol, 64980-438 — Atenolol, 64980-439 — Atenolol, 65841-023 — Atenolol, 65841-024 — Atenolol, 65862-168 — Atenolol, 65862-169 — Atenolol, 65862-170 — Atenolol, 66267-029 — Atenolol, 67046-0663 — Atenolol, 67046-0843 — Atenolol, 67046-1076 — Atenolol, 68071-3694 — 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.