Escitalopram
NDC 51672-1348 · Sun Pharmaceutical Industries, Inc.
Packages
51672-1348-1 — 1 BOTTLE in 1 CARTON (51672-1348-1) / 240 mL in 1 BOTTLE
51672-1348-8 — 1 BOTTLE in 1 CARTON (51672-1348-8) / 120 mL in 1 BOTTLE
51672-1348-9 — 1 BOTTLE in 1 CARTON (51672-1348-9) / 480 mL in 1 BOTTLE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
50090-7200 — Escitalopram Oxalate, 50090-7201 — Escitalopram Oxalate, 51655-116 — Escitalopram, 51655-147 — Escitalopram Oxalate, 51655-149 — Escitalopram, 51655-236 — Escitalopram, 51655-277 — Escitalopram, 51655-284 — Escitalopram, 51655-449 — Escitalopram, 51655-766 — Escitalopram, 52427-795 — escitalopram, 53746-019 — Escitalopram Oxalate, 53746-020 — Escitalopram Oxalate, 53746-021 — Escitalopram Oxalate, 55154-6893 — escitalopram, 55154-7288 — escitalopram, 59746-279 — Escitalopram Oxalate, 59746-280 — Escitalopram Oxalate, 59746-281 — Escitalopram Oxalate, 60687-865 — Escitalopram, +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