Citalopram Hydrobromide

NDC 72657-111 · Glenmark Therapeutics Inc., USA

Generic nameCitalopram Hydrobromide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CITALOPRAM HYDROBROMIDE

Strength40 mg/1

Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Marketing categoryANDA

Packages

72657-111-01 — 100 TABLET, FILM COATED in 1 BOTTLE (72657-111-01)

72657-111-05 — 500 TABLET, FILM COATED in 1 BOTTLE (72657-111-05)

FDA lists these products with the same active ingredient.

71335-0480 — Citalopram Hydrobromide, 71335-2232 — citalopram, 71610-092 — CITALOPRAM, 71610-412 — Citalopram, 71610-413 — Citalopram Hydrobromide, 71610-422 — Citalopram, 72162-2517 — Citalopram Hydrobromide, 72162-2567 — Citalopram, 72657-109 — Citalopram Hydrobromide, 72657-110 — Citalopram Hydrobromide, 72789-071 — Citalopram, 76282-208 — CITALOPRAM, 76282-628 — CITALOPRAM, 76282-629 — CITALOPRAM, 80425-0093 — Citalopram, 80425-0309 — Citalopram Hydrobromide, 80425-0557 — Citalopram, 82009-106 — Citalopram Hydrobromide, 82009-107 — Citalopram Hydrobromide, 82009-108 — Citalopram Hydrobromide, +99 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.