Escitalopram

NDC 51655-149 · Northwind Health Company, 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

51655-149-26 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-26)

51655-149-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52)

FDA lists these products with the same active ingredient.

50090-6190 — Escitalopram, 50090-6191 — Escitalopram, 50090-6496 — Escitalopram Oxalate, 50090-6534 — Escitalopram, 50090-6897 — Escitalopram, 50090-7177 — escitalopram, 50090-7200 — Escitalopram Oxalate, 50090-7201 — Escitalopram Oxalate, 51655-116 — Escitalopram, 51655-147 — Escitalopram Oxalate, 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, +133 more

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