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Escitalopram

NDC 71335-1241 · Bryant Ranch Prepack

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

71335-1241-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-1241-1)

71335-1241-2 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-1241-2)

71335-1241-3 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-1241-3)

71335-1241-4 — 100 TABLET, FILM COATED in 1 BOTTLE (71335-1241-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-313 — escitalopram oxalate, 71205-325 — Escitalopram, 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, 71335-1307 — Escitalopram, 71335-2058 — Escitalopram, 71335-2331 — escitalopram, 71335-2460 — escitalopram, 71335-2903 — escitalopram, 71335-2960 — escitalopram, 71335-3094 — escitalopram, 71335-9687 — Escitalopram Oxalate, 71610-425 — Escitalopram, 71610-534 — 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.