Escitalopram

NDC 68071-5248 · NuCare 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

68071-5248-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68071-5248-3)

68071-5248-9 — 90 TABLET, FILM COATED in 1 BOTTLE (68071-5248-9)

FDA lists these products with the same active ingredient.

65862-375 — Escitalopram Oxalate, 67046-0355 — Escitalopram, 67046-1465 — escitalopram, 67046-1472 — escitalopram, 67296-1421 — Escitalopram, 68001-591 — Escitalopram, 68001-592 — Escitalopram, 68001-593 — Escitalopram, 68071-3069 — Escitalopram, 68071-4985 — 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, 68788-8723 — 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.