Skip to main content

escitalopram

NDC 68788-8723 · Preferred Pharmaceuticals Inc.

Generic nameescitalopram
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

68788-8723-1 — 100 TABLET, FILM COATED in 1 BOTTLE (68788-8723-1)

68788-8723-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8723-3)

68788-8723-6 — 60 TABLET, FILM COATED in 1 BOTTLE (68788-8723-6)

68788-8723-8 — 28 TABLET, FILM COATED in 1 BOTTLE (68788-8723-8)

68788-8723-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68788-8723-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-5248 — Escitalopram, 68084-617 — Escitalopram Oxalate, 68084-618 — Escitalopram Oxalate, 68180-137 — Escitslopram, 68645-519 — Escitalopram, 68645-520 — Escitalopram, 68788-4171 — escitalopram, 68788-7461 — Escitalopram, 68788-8371 — escitalopram oxalate, 68788-8569 — 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, 70518-4300 — 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.