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escitalopram oxalate

NDC 82009-037 · Quallent Pharmaceuticals Health LLC

Generic nameescitalopram oxalate
Dosage formTABLET
RouteORAL
Active ingredient(s)ESCITALOPRAM OXALATE
Strength20 mg/1
Pharmacologic classSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

82009-037-10 — 1000 TABLET in 1 BOTTLE (82009-037-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 76282-249 — escitalopram, 76282-250 — escitalopram, 76282-251 — escitalopram, 76420-721 — Escitalopram Oxalate, 76420-722 — Escitalopram Oxalate, 76420-723 — Escitalopram Oxalate, 80425-0320 — Escitalopram, 80425-0375 — Escitalopram Oxalate, 82009-035 — escitalopram oxalate, 82009-036 — 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.