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TENORMIN

NDC 24979-244 · Upsher-Smith Laboratories, LLC

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

Packages

24979-244-07 — 90 TABLET in 1 BOTTLE (24979-244-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-0757 — atenolol, 0591-5782 — Atenolol and Chlorthalidone, 0591-5783 — Atenolol and Chlorthalidone, 0615-8372 — Atenolol, 0615-8373 — Atenolol, 0904-7187 — Atenolol, 10135-733 — atenolol and chlorthalidone tablet, 10135-734 — atenolol and chlorthalidone tablet, 16714-936 — Atenolol and Chlorthalidone, 16714-937 — Atenolol and Chlorthalidone, 24979-245 — Atenolol, 24979-246 — Atenolol, 24979-256 — Atenolol and Chlorthalidone, 24979-257 — Atenolol and Chlorthalidone, 29300-400 — Atenolol and Chlorthalidone, 29300-401 — Atenolol and Chlorthalidone, 29300-410 — Atenolol, 29300-411 — Atenolol, 29300-412 — Atenolol, 42708-012 — 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.