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Escitalopram

NDC 50090-6534 · A-S Medication Solutions

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

50090-6534-0 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)

50090-6534-1 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 50090-6496 — Escitalopram Oxalate, 50090-6897 — Escitalopram, 50090-7177 — escitalopram, 50090-7200 — Escitalopram Oxalate, 50090-7201 — Escitalopram Oxalate, 51655-116 — Escitalopram, 51655-147 — Escitalopram Oxalate, 51655-149 — Escitalopram, 51655-236 — Escitalopram, 51655-277 — Escitalopram, 51655-284 — Escitalopram, +133 more

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