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Chlorthalidone

NDC 16714-129 · Northstar Rx LLC.

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

Packages

16714-129-01 — 100 TABLET in 1 BOTTLE (16714-129-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-0213 — chlorthalidone, 0378-0222 — chlorthalidone, 0591-5782 — Atenolol and Chlorthalidone, 0591-5783 — Atenolol and Chlorthalidone, 0904-6900 — Chlorthalidone, 0904-7583 — chlorthalidone, 10135-733 — atenolol and chlorthalidone tablet, 10135-734 — atenolol and chlorthalidone tablet, 16714-128 — Chlorthalidone, 16714-936 — Atenolol and Chlorthalidone, 16714-937 — Atenolol and Chlorthalidone, 24979-256 — Atenolol and Chlorthalidone, 24979-257 — Atenolol and Chlorthalidone, 27241-216 — Chlorthalidone, 27241-217 — Chlorthalidone, 29300-333 — Chlorthalidone, 29300-334 — Chlorthalidone, 29300-400 — Atenolol and Chlorthalidone, 29300-401 — Atenolol and Chlorthalidone, 33342-425 — 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.