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Escitalopram Oxalate

NDC 65162-020 · Amneal Pharmaceuticals LLC

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

65162-020-03 — 30 TABLET, FILM COATED in 1 BOTTLE (65162-020-03)

65162-020-09 — 90 TABLET, FILM COATED in 1 BOTTLE (65162-020-09)

65162-020-11 — 1000 TABLET, FILM COATED in 1 BOTTLE (65162-020-11)

65162-020-50 — 500 TABLET, FILM COATED in 1 BOTTLE (65162-020-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-7288 — escitalopram, 59746-279 — Escitalopram Oxalate, 59746-280 — Escitalopram Oxalate, 59746-281 — Escitalopram Oxalate, 60687-865 — Escitalopram, 60760-590 — Escitalopram Oxalate, 60760-894 — escitalopram, 60760-895 — escitalopram, 62135-729 — Escitalopram Oral, 65162-019 — Escitalopram Oxalate, 65162-021 — Escitalopram Oxalate, 65162-705 — Escitalopram, 65862-248 — Escitalopram Oxalate, 65862-373 — Escitalopram Oxalate, 65862-374 — Escitalopram Oxalate, 65862-375 — Escitalopram Oxalate, 67046-0355 — Escitalopram, 67046-1465 — escitalopram, 67046-1472 — escitalopram, 67296-1421 — 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.