Escitalopram

NDC 43547-280 · SOLCO HEALTHCARE US, LLC

Generic nameEscitalopram

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ESCITALOPRAM OXALATE

Strength5 mg/1

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

Marketing categoryANDA

Packages

43547-280-10 — 100 TABLET, FILM COATED in 1 BOTTLE (43547-280-10)

43547-280-11 — 1000 TABLET, FILM COATED in 1 BOTTLE (43547-280-11)

FDA lists these products with the same active ingredient.

31722-569 — Escitalopram Oxalate, 33342-036 — Escitalopram Oxalate, 33342-037 — Escitalopram Oxalate, 33342-038 — Escitalopram Oxalate, 33342-053 — escitalopram, 42708-077 — Escitalopram Oxalate, 42708-155 — Escitalopram, 42708-163 — Escitalopram, 43063-661 — Escitalopram, 43063-761 — escitalopram oxalate, 43547-281 — Escitalopram, 43547-282 — Escitalopram, 43602-473 — escitalopram, 43602-474 — escitalopram, 43602-475 — escitalopram, 50090-4915 — Escitalopram, 50090-5312 — Escitalopram, 50090-6023 — Escitalopram Oxalate, 50090-6190 — Escitalopram, 50090-6191 — 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.