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Escitalopram Oxalate

NDC 68645-519 · Legacy Pharmaceutical Packaging, LLC

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

68645-519-54 — 30 TABLET, FILM COATED in 1 BOTTLE (68645-519-54)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-1421 — Escitalopram, 68001-591 — Escitalopram, 68001-592 — Escitalopram, 68001-593 — Escitalopram, 68071-3069 — Escitalopram, 68071-4985 — Escitalopram, 68071-5248 — Escitalopram, 68084-617 — Escitalopram Oxalate, 68084-618 — Escitalopram Oxalate, 68180-137 — Escitslopram, 68645-520 — Escitalopram, 68788-4171 — escitalopram, 68788-7461 — Escitalopram, 68788-8371 — escitalopram oxalate, 68788-8569 — escitalopram, 68788-8723 — escitalopram, 68999-729 — Escitalopram Oral, 69097-847 — Escitalopram, 69097-848 — Escitalopram, 69097-849 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels