lexapro

Generic: escitalopram

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lexapro
Generic Name escitalopram
Labeler allergan, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0456-2010
Product ID 0456-2010_9ff46a66-0f97-4a78-9d18-ec576f63bae7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021323
Listing Expiration 2026-12-31
Marketing Start 2002-08-14

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04562010
Hyphenated Format 0456-2010

Supplemental Identifiers

RxCUI
349332 351249 351250 351285 352272 352273 404408 404420
UNII
5U85DBW7LO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lexapro (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number NDA021323 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0456-2010-01)
source: ndc

Packages (1)

0456-2010-01 100 TABLET, FILM COATED in 1 BOTTLE (0456-2010-01)

Ingredients (1)

escitalopram oxalate (10 mg/1)

Linked Drug Pages (1)

Lexapro ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9ff46a66-0f97-4a78-9d18-ec576f63bae7", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250", "351285", "352272", "352273", "404408", "404420"], "spl_set_id": ["13bb8267-1cab-43e5-acae-55a4d957630a"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0456-2010-01)", "package_ndc": "0456-2010-01", "marketing_start_date": "20020814"}], "brand_name": "Lexapro", "product_id": "0456-2010_9ff46a66-0f97-4a78-9d18-ec576f63bae7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0456-2010", "generic_name": "ESCITALOPRAM", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lexapro", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "NDA021323", "marketing_category": "NDA", "marketing_start_date": "20020814", "listing_expiration_date": "20261231"}