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escitalopram oxalate

NDC 71335-0322 · Bryant Ranch Prepack

Generic nameescitalopram oxalate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ESCITALOPRAM OXALATE
Strength10 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

71335-0322-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0322-1)

71335-0322-2 28 TABLET, FILM COATED in 1 BOTTLE (71335-0322-2)

71335-0322-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-0322-3)

71335-0322-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-0322-4)

71335-0322-5 10 TABLET, FILM COATED in 1 BOTTLE (71335-0322-5)

71335-0322-6 120 TABLET, FILM COATED in 1 BOTTLE (71335-0322-6)

71335-0322-7 7 TABLET, FILM COATED in 1 BOTTLE (71335-0322-7)

71335-0322-8 180 TABLET, FILM COATED in 1 BOTTLE (71335-0322-8)

71335-0322-9 100 TABLET, FILM COATED in 1 BOTTLE (71335-0322-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4300 — escitalopram, 70518-4567 — Escitalopram, 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, 71335-0685 — escitalopram oxalate, 71335-1002 — Escitalopram, 71335-1030 — Escitalopram, 71335-1187 — Escitalopram, 71335-1241 — Escitalopram, 71335-1307 — Escitalopram, 71335-2058 — Escitalopram, 71335-2331 — escitalopram, 71335-2460 — escitalopram, 71335-2903 — 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.