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United States · US · US:0456-2020_9ff46a66-0f97-4a78-9d18-ec576f63bae7

Lexapro

Orange BookUNIISPLATC N06AB10

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeN06AB10
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0456202001
    100 TABLET, FILM COATED in 1 BOTTLE (0456-2020-01)

Annotations

UNII (FDA Substance ID)
5U85DBW7LO
ESCITALOPRAM OXALATE
RxCUI 353108
Orange Book
N021323
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5U85DBW7LO",
    "rxcui": "353108",
    "inchikey": "KTGRHKOEFSJQNS-BDQAORGHSA-N",
    "display_name": "ESCITALOPRAM OXALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "13bb8267-1cab-43e5-acae-55a4d957630a": {
      "match": "brand_token",
      "title": "LEXAPRO (ESCITALOPRAM) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM) SOLUTION [ALLERGAN, INC.]",
      "spl_version": "45",
      "published_date": "2026-01-01"
    }
  },
  "productid": "0456-2020_9ff46a66-0f97-4a78-9d18-ec576f63bae7",
  "productndc": "0456-2020",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "021323",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 5MG BASE",
        "product_no": "001",
        "approval_date": "Aug 14, 2002"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "002",
        "approval_date": "Aug 14, 2002"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "003",
        "approval_date": "Aug 14, 2002"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ESCITALOPRAM OXALATE",
  "proprietary_name": "Lexapro",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA021323",
  "marketing_category": "NDA",
  "nonproprietary_name": "ESCITALOPRAM",
  "start_marketing_date": "20020814",
  "active_numerator_strength": "20"
}

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