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Escitalopram

NDC 68001-592 · BluePoint Laboratories

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

68001-592-00 — 100 TABLET, FILM COATED in 1 BOTTLE (68001-592-00)

68001-592-08 — 1000 TABLET, FILM COATED in 1 BOTTLE (68001-592-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68001-591 — Escitalopram, 68001-593 — Escitalopram, 68071-3069 — Escitalopram, 68071-4985 — Escitalopram, 68071-5248 — Escitalopram, 68084-617 — Escitalopram Oxalate, 68084-618 — Escitalopram Oxalate, 68180-137 — Escitslopram, 68645-519 — Escitalopram, 68645-520 — Escitalopram, 68788-4171 — 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.