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Citalopram Hydrobromide

NDC 71205-764 · Proficient Rx LP

Generic nameCitalopram Hydrobromide
Dosage formTABLET
RouteORAL
Active ingredient(s)CITALOPRAM HYDROBROMIDE
Strength40 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

71205-764-30 — 30 TABLET in 1 BOTTLE (71205-764-30)

71205-764-60 — 60 TABLET in 1 BOTTLE (71205-764-60)

71205-764-90 — 90 TABLET in 1 BOTTLE (71205-764-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69097-824 — Citalopram, 70518-2228 — Citalopram, 70518-2553 — citalopram, 70518-2601 — citalopram, 70518-2617 — Citalopram, 70518-4114 — Citalopram Hydrobromide, 70518-4334 — Citalopram Hydrobromide, 70518-4335 — Citalopram, 70518-4416 — Citalopram, 70518-4476 — Citalopram, 71335-0238 — Citalopram Hydrobromide, 71335-0377 — Citalopram, 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, +99 more

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