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Escitalopram

NDC 71335-1002 · Bryant Ranch Prepack

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

71335-1002-1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1002-1)

71335-1002-2 28 TABLET, FILM COATED in 1 BOTTLE (71335-1002-2)

71335-1002-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-1002-3)

71335-1002-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1002-4)

71335-1002-5 120 TABLET, FILM COATED in 1 BOTTLE (71335-1002-5)

71335-1002-6 100 TABLET, FILM COATED in 1 BOTTLE (71335-1002-6)

71335-1002-7 45 TABLET, FILM COATED in 1 BOTTLE (71335-1002-7)

71335-1002-8 180 TABLET, FILM COATED in 1 BOTTLE (71335-1002-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4703 — Escitalopram, 71205-168 — Escitalopram Oxalate, 71205-193 — Escitalopram Oxalate, 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, 71335-1030 — Escitalopram, 71335-1187 — Escitalopram, 71335-1241 — Escitalopram, 71335-1307 — Escitalopram, 71335-2058 — Escitalopram, 71335-2331 — escitalopram, 71335-2460 — escitalopram, 71335-2903 — escitalopram, 71335-2960 — escitalopram, 71335-3094 — 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.