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Escitalopram

NDC 60687-865 · American Health Packaging

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

60687-865-01 — 100 BLISTER PACK in 1 CARTON (60687-865-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-865-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51672-1348 — Escitalopram Oxalate, 52427-795 — escitalopram, 53746-019 — Escitalopram Oxalate, 53746-020 — Escitalopram Oxalate, 53746-021 — Escitalopram Oxalate, 55154-6893 — escitalopram, 55154-7288 — escitalopram, 59746-279 — Escitalopram Oxalate, 59746-280 — Escitalopram Oxalate, 59746-281 — Escitalopram Oxalate, 60760-590 — Escitalopram Oxalate, 60760-894 — escitalopram, 60760-895 — escitalopram, 62135-729 — Escitalopram Oral, 65162-019 — Escitalopram Oxalate, 65162-020 — Escitalopram Oxalate, 65162-021 — Escitalopram Oxalate, 65162-705 — Escitalopram, 65862-248 — Escitalopram Oxalate, 65862-373 — 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.