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escitalopram

NDC 72162-2241 · Bryant Ranch Prepack

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

72162-2241-0 — 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2241-0)

72162-2241-1 — 100 TABLET, FILM COATED in 1 BOTTLE (72162-2241-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2058 — Escitalopram, 71335-2331 — escitalopram, 71335-2460 — escitalopram, 71335-2903 — escitalopram, 71335-2960 — escitalopram, 71335-3094 — escitalopram, 71335-9687 — Escitalopram Oxalate, 71610-425 — Escitalopram, 71610-534 — escitalopram, 72162-2240 — escitalopram, 72162-2242 — escitalopram, 72189-424 — Escitalopram, 72189-438 — Escitalopram, 72189-449 — Escitalopram, 72189-451 — Escitalopram, 72603-149 — Escitalopram Oxalate, 72603-150 — Escitalopram Oxalate, 72603-151 — Escitalopram Oxalate, 72789-194 — Escitalopram, 72789-311 — Escitalopram Oxalate, +133 more

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