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Escitalopram

NDC 72189-449 · Direct_Rx

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

72189-449-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72189-449-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2960 — escitalopram, 71335-3094 — escitalopram, 71335-9687 — Escitalopram Oxalate, 71610-425 — Escitalopram, 71610-534 — escitalopram, 72162-2240 — escitalopram, 72162-2241 — escitalopram, 72162-2242 — escitalopram, 72189-424 — Escitalopram, 72189-438 — Escitalopram, 72189-451 — Escitalopram, 72603-149 — Escitalopram Oxalate, 72603-150 — Escitalopram Oxalate, 72603-151 — Escitalopram Oxalate, 72789-194 — Escitalopram, 72789-311 — Escitalopram Oxalate, 76282-249 — escitalopram, 76282-250 — escitalopram, 76282-251 — escitalopram, 76420-721 — Escitalopram Oxalate, +133 more

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