Skip to main content

Citalopram Hydrobromide

NDC 55700-787 · Quality Care Products, LLC

Generic nameCitalopram Hydrobromide
Dosage formTABLET
RouteORAL
Active ingredient(s)CITALOPRAM HYDROBROMIDE
Strength10 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

55700-787-30 — 30 TABLET in 1 BOTTLE (55700-787-30)

55700-787-90 — 90 TABLET in 1 BOTTLE (55700-787-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 55700-851 — Citalopram Hydrobromide, 59651-964 — CITALOPRAM, 60429-175 — citalopram, 60760-009 — Citalopram, 60760-495 — Citalopram, 62135-540 — Citalopram, 63187-140 — Citalopram Hydrobromide, 63187-203 — Citalopram Hydrobromide, 63187-220 — Citalopram Hydrobromide, 63187-679 — Citalopram Hydrobromide, +99 more

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