Skip to main content

Citalopram Hydrobromide

NDC 68788-8962 · Preferred Pharmaceuticals Inc.

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

68788-8962-1 — 100 TABLET, FILM COATED in 1 BOTTLE (68788-8962-1)

68788-8962-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8962-3)

68788-8962-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68788-8962-6)

68788-8962-8 — 120 TABLET, FILM COATED in 1 CARTON (68788-8962-8)

68788-8962-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68788-8962-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-0795 — Citalopram, 68071-1830 — Citalopram Hydrobromide, 68071-1906 — Citalopram Hydrobromide, 68071-2198 — Citalopram Hydrobromide, 68071-2459 — Citalopram Hydrobromide, 68071-3357 — Citalopram Hydrobromide, 68071-3384 — Citalopram Hydrobromide, 68071-3558 — citalopram, 68071-5132 — Citalopram Hydrobromide, 68788-0802 — Citalopram Hydrobromide, 68788-9692 — Citalopram Hydrobromide, 68999-540 — Citalopram, 69097-822 — Citalopram, 69097-823 — Citalopram, 69097-824 — Citalopram, 70518-2228 — Citalopram, 70518-2553 — citalopram, 70518-2601 — citalopram, 70518-2617 — Citalopram, 70518-4114 — 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.