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Prescription medicine · generic available

Escitalopram

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Escitalopram used for?
The FDA-approved label (Lexapro, Allergan, Inc., October 1, 2023) says: “Lexapro is indicated for the treatment of: • major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. • generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older. Lexapro is a selective serotonin reuptake inhibitor (SSRI) indicated for the …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Escitalopram have a boxed warning?
Yes. The FDA label for Lexapro has a boxed warning (“WARNING: SUICIDAL THOUGHTS AND BEHAVIORS”), the FDA’s strongest warning. Read it on the full label and ask your pharmacist.
Is there a shortage of Escitalopram?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Escitalopram been recalled?
FDA enforcement reports list 1 recall of products of this medicine; the newest started March 24, 2016 (Class III). A recall usually concerns specific lots, not every product.
Who makes Escitalopram?
42 companies list prescription products of Escitalopram in the FDA NDC Directory, including Bryant Ranch Prepack, A-S Medication Solutions and Northwind Health Company, LLC.

What Escitalopram is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

Lexapro is indicated for the treatment of: • major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. • generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older. Lexapro is a selective serotonin reuptake inhibitor (SSRI) indicated for the …

— FDA label: Lexapro, Allergan, Inc., effective October 1, 2023. Read the full label on DailyMed →

The FDA has 107 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Conditions named on the label

These condition names appear word for word in the label’s “Indications and Usage” text (matched with a reviewed table). Each page lists hospitals whose own websites name the condition.

Related medical specialties

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

This label has a boxed warning. Its heading: WARNING: SUICIDAL THOUGHTS AND BEHAVIORS. Read it on the full label →

107 of 107 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsTablet, film coated · Tablet · Solution · Capsule
RouteOral
Prescription products155 in the FDA NDC Directory
Brand namesLexapro

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Escitalopram, by strength and form
Strength and formGeneric or brandPharmacies pay
escitalopram oxalate 10 mg
tablet
Generic $0.0391 per tablet
escitalopram oxalate 10 mg
tablet, film coated
Generic $0.0391 per tablet
escitalopram oxalate 10 mg
tablet, film coated
Brand: Lexapro $15.43 per tablet
escitalopram oxalate 10 mg/21
tablet, film coated
Generic $0.0391 per tablet
escitalopram oxalate 15 mg
capsule
Generic $5.51 per capsule
escitalopram oxalate 20 mg
tablet
Generic $0.0632 per tablet
escitalopram oxalate 20 mg
tablet, film coated
Generic $0.0632 per tablet
escitalopram oxalate 20 mg
tablet, film coated
Brand: Lexapro $16.11 per tablet
escitalopram oxalate 20 mg/21
tablet, film coated
Generic $0.0632 per tablet
escitalopram oxalate 5 mg
tablet
Generic $0.0429 per tablet
escitalopram oxalate 5 mg
tablet, film coated
Generic $0.0429 per tablet
escitalopram oxalate 5 mg
tablet, film coated
Brand: Lexapro $14.74 per tablet
escitalopram oxalate 5 mg/5 mL
solution
Generic $0.1608 per mL

NADAC list of November 4, 2026; these prices took effect between January 2, 2026 and October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA021323
LEXAPRO
AbbvieAugust 14, 2002 29, latest April 19, 2024
2024: Labeling · 2023: Labeling · 2023: Efficacy
NDA219130
ESCITALOPRAM
AlmaticaAugust 29, 2025 —

Generic approvals (16)

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

From FDA enforcement reports, matched by the product’s NDC code. A recall usually covers specific lots only: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.

  1. March 24, 2016 · Class III · Terminated · D-1516-201

    Labeling: Incorrect or Missing Lot and/or Expiration Date

    Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 21202, Manufactured by: Lupin Limited, Goa 403 722, India, NDC 68180-136-01 — Lupin Limited

What do the recall classes mean?

Class I: The most serious type: there is a reasonable chance that using the product will cause serious health problems or death.
Class II: Using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
Class III: Using the product is not likely to cause health problems (for example a labeling or packaging issue).

Official identifiers

RxCUI (RxNorm)349332, 351249, 351250, 351285, 352272, 352273, 404408, 404420, 2725159
SPL set ID of the quoted label13bb8267-1cab-43e5-acae-55a4d957630a
FDA labels (SPL)107
FDA applicationsNDA021323, NDA219130, 16 ANDA
Active ingredients (FDA)ESCITALOPRAM

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Lexapro, Allergan, Inc., effective October 1, 2023; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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