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escitalopram

NDC 60760-895 · St. Mary's Medical Park Pharmacy

Generic nameescitalopram
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

60760-895-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-30)

60760-895-90 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 60687-865 — Escitalopram, 60760-590 — Escitalopram Oxalate, 60760-894 — 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, 65862-374 — Escitalopram Oxalate, 65862-375 — Escitalopram Oxalate, 67046-0355 — 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.