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Escitalopram

NDC 59746-281 · Jubilant Cadista Pharmaceuticals Inc.

Generic nameEscitalopram Oxalate
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

59746-281-01 — 100 TABLET, FILM COATED in 1 BOTTLE (59746-281-01)

59746-281-05 — 500 TABLET, FILM COATED in 1 BOTTLE (59746-281-05)

59746-281-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (59746-281-10)

59746-281-30 — 30 TABLET, FILM COATED in 1 BOTTLE (59746-281-30)

59746-281-90 — 90 TABLET, FILM COATED in 1 BOTTLE (59746-281-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-766 — Escitalopram, 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, 60687-865 — Escitalopram, 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, +133 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.