Citalopram Hydrobromide

NDC 51655-043 · Northwind Health Company, LLC

Generic nameCitalopram Hydrobromide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CITALOPRAM HYDROBROMIDE

Strength10 mg/1

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

Marketing categoryANDA

Packages

51655-043-26 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-26)

51655-043-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-52)

FDA lists these products with the same active ingredient.

50090-3136 — Citalopram Hydrobromide, 50090-3208 — Citalopram Hydrobromide, 50090-5170 — Citalopram, 50090-5172 — Citalopram, 50090-5175 — Citalopram, 50090-6433 — Citalopram Hydrobromide, 50090-6846 — Citalopram Hydrobromide, 50090-6947 — Citalopram Hydrobromide, 50090-7039 — Citalopram Hydrobromide, 50090-7419 — Citalopram Hydrobromide, 51655-137 — Citalopram, 51655-209 — Citalopram, 51655-605 — Citalopram Hydrobromide, 51655-664 — Citalopram, 51655-667 — Citalopram, 51655-680 — Citalopram Hydrobromide, 51655-938 — Citalopram, 52427-691 — citalopram, 55154-3329 — Citalopram, 55154-3349 — Citalopram, +99 more

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