Escitalopram

NDC 71205-325 · Proficient Rx LP

Generic nameEscitalopram

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESCITALOPRAM OXALATE

Strength20 mg/1

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

Marketing categoryANDA

Packages

71205-325-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30)

71205-325-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)

71205-325-90 — 90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)

FDA lists these products with the same active ingredient.

70518-2472 — Escitalopram, 70518-2597 — Escitalopram, 70518-3923 — escitalopram, 70518-4239 — escitalopram, 70518-4300 — escitalopram, 70518-4567 — Escitalopram, 70518-4703 — Escitalopram, 71205-168 — Escitalopram Oxalate, 71205-193 — Escitalopram Oxalate, 71205-313 — escitalopram oxalate, 71205-344 — Escitalopram, 71205-782 — Escitalopram, 71205-792 — escitalopram oxalate, 71335-0322 — escitalopram oxalate, 71335-0685 — escitalopram oxalate, 71335-1002 — Escitalopram, 71335-1030 — Escitalopram, 71335-1187 — Escitalopram, 71335-1241 — Escitalopram, 71335-1307 — Escitalopram, +133 more

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