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Chlorthalidone

NDC 57664-649 · Sun Pharmaceutical Industries, Inc.

Generic nameChlorthalidone
Dosage formTABLET
RouteORAL
Active ingredient(s)CHLORTHALIDONE
Strength50 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide-like Diuretic [EPC]
Marketing categoryANDA

Packages

57664-649-18 — 1000 TABLET in 1 BOTTLE (57664-649-18)

57664-649-88 — 100 TABLET in 1 BOTTLE (57664-649-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51224-018 — Chlorthalidone, 51224-118 — Chlorthalidone, 51655-477 — CHLORTHALIDONE, 51655-526 — CHLORTHALIDONE, 51655-790 — Chlorthalidone, 51655-961 — Chlorthalidone, 51655-992 — Chlorthalidone, 55289-067 — chlorthalidone, 55289-993 — Atenolol and Chlorthalidone, 57664-648 — Chlorthalidone, 59746-760 — Chlorthalidone, 59746-761 — Chlorthalidone, 60290-004 — Chlorthalidone, 60290-005 — Chlorthalidone, 60631-412 — Azilsartan kamedoxomil and chlorthalidone, 60631-425 — Azilsartan kamedoxomil and chlorthalidone, 60687-317 — Chlorthalidone, 62135-505 — Chlorthalidone, 62135-506 — Chlorthalidone, 62332-676 — CHLORTHALIDONE, +102 more

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