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escitalopram

NDC 70518-4300 · REMEDYREPACK INC.

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

70518-4300-0 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4300-0)

70518-4300-1 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4300-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8723 — escitalopram, 68999-729 — Escitalopram Oral, 69097-847 — Escitalopram, 69097-848 — Escitalopram, 69097-849 — Escitalopram, 70518-2317 — Escitalopram, 70518-2472 — Escitalopram, 70518-2597 — Escitalopram, 70518-3923 — escitalopram, 70518-4239 — escitalopram, 70518-4567 — Escitalopram, 70518-4703 — Escitalopram, 71205-168 — Escitalopram Oxalate, 71205-193 — Escitalopram Oxalate, 71205-313 — escitalopram oxalate, 71205-325 — Escitalopram, 71205-344 — Escitalopram, 71205-782 — Escitalopram, 71205-792 — escitalopram oxalate, 71335-0322 — 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.