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Escitalopram oxalate

NDC 71610-534 · Aphena Pharma Solutions - Tennessee, LLC

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

71610-534-60 — 90 TABLET, FILM COATED in 1 BOTTLE (71610-534-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1241 — 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, 72162-2240 — escitalopram, 72162-2241 — escitalopram, 72162-2242 — escitalopram, 72189-424 — Escitalopram, 72189-438 — Escitalopram, 72189-449 — Escitalopram, 72189-451 — Escitalopram, 72603-149 — Escitalopram Oxalate, 72603-150 — Escitalopram Oxalate, 72603-151 — 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.