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CHLORTHALIDONE

NDC 46708-676 · Alembic Pharmaceuticals Limited

Generic nameCHLORTHALIDONE
Dosage formTABLET
RouteORAL
Active ingredient(s)CHLORTHALIDONE
Strength25 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide-like Diuretic [EPC]
Marketing categoryANDA

Packages

46708-676-31 — 100 TABLET in 1 BOTTLE (46708-676-31)

46708-676-90 — 90 TABLET in 1 BOTTLE (46708-676-90)

46708-676-91 — 1000 TABLET in 1 BOTTLE (46708-676-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-333 — Chlorthalidone, 29300-334 — Chlorthalidone, 29300-400 — Atenolol and Chlorthalidone, 29300-401 — Atenolol and Chlorthalidone, 33342-425 — Chlorthalidone, 33342-426 — Chlorthalidone, 43598-167 — CHLORTHALIDONE, 43598-170 — CHLORTHALIDONE, 43598-719 — CHLORTHALIDONE, 43598-720 — CHLORTHALIDONE, 46708-677 — CHLORTHALIDONE, 48433-021 — chlorthalidone, 50090-5183 — Chlorthalidone, 50090-5643 — Chlorthalidone, 50090-6126 — Chlorthalidone, 50090-6957 — Chlorthalidone, 50090-6958 — Chlorthalidone, 50090-7831 — Chlorthalidone, 50268-167 — CHLORTHALIDONE, 50742-285 — 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.