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Escitalopram

NDC 0615-8477 · NCS HealthCare of KY, LLC dba Vangard Labs

Generic nameEscitalopram Oxalate
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

0615-8477-05 — 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-05)

0615-8477-39 — 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-39)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0456-2005 — ESCITALOPRAM, 0456-2010 — ESCITALOPRAM, 0456-2020 — ESCITALOPRAM, 0615-8475 — Escitalopram Oxalate, 0615-8476 — Escitalopram Oxalate, 0904-6426 — escitalopram, 0904-6427 — escitalopram, 13668-135 — escitalopram, 13668-136 — escitalopram, 13668-137 — escitalopram, 16571-755 — escitalopram, 16571-756 — escitalopram, 16571-757 — escitalopram, 16571-769 — Escitalopram Oxalate, 16729-168 — Escitalopram, 16729-169 — Escitalopram, 16729-170 — Escitalopram, 31722-569 — Escitalopram Oxalate, 33342-036 — Escitalopram Oxalate, 33342-037 — 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.