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Atenolol and Chlorthalidone

NDC 70710-1167 · Zydus Pharmaceuticals USA Inc.

Generic nameAtenolol and Chlorthalidone
Dosage formTABLET
RouteORAL
Active ingredient(s)ATENOLOL, CHLORTHALIDONE
Strength50; 25 mg/1; mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

70710-1167-1 — 100 TABLET in 1 BOTTLE (70710-1167-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8834 — Atenolol, 70199-017 — Chlorthalidone, 70518-3036 — Atenolol, 70518-3531 — Atenolol, 70518-3718 — chlorthalidone, 70518-3954 — Chlorthalidone, 70518-4099 — Atenolol, 70518-4111 — Atenolol and Chlorthalidone, 70518-4287 — Atenolol, 70518-4578 — Chlorthalidone, 70710-1168 — Atenolol and Chlorthalidone, 70756-011 — chlorthalidone, 70756-020 — chlorthalidone, 70771-1369 — Chlorthalidone, 70771-1370 — Chlorthalidone, 70771-1372 — Atenolol and Chlorthalidone, 70771-1373 — Atenolol and Chlorthalidone, 70954-390 — Atenolol and Chlorthalidone, 70954-391 — Atenolol and Chlorthalidone, 71205-096 — Atenolol, +228 more

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