escitalopram

NDC 55154-6893 · Cardinal Health 107, LLC

Generic nameescitalopram

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESCITALOPRAM OXALATE

Strength10 mg/1

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

Marketing categoryANDA

Packages

55154-6893-0 — 10 BLISTER PACK in 1 BAG (55154-6893-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

51655-236 — Escitalopram, 51655-277 — Escitalopram, 51655-284 — Escitalopram, 51655-449 — Escitalopram, 51655-766 — Escitalopram, 51672-1348 — Escitalopram Oxalate, 52427-795 — escitalopram, 53746-019 — Escitalopram Oxalate, 53746-020 — Escitalopram Oxalate, 53746-021 — Escitalopram Oxalate, 55154-7288 — escitalopram, 59746-279 — Escitalopram Oxalate, 59746-280 — Escitalopram Oxalate, 59746-281 — Escitalopram Oxalate, 60687-865 — Escitalopram, 60760-590 — Escitalopram Oxalate, 60760-894 — escitalopram, 60760-895 — escitalopram, 62135-729 — Escitalopram Oral, 65162-019 — Escitalopram Oxalate, +133 more

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