Escitalopram

Orange BookUNIISPLATC N06AB10

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AB10

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133510021
60 TABLET, FILM COATED in 1 BOTTLE (71335-1002-1)
ndc11
7133510022
28 TABLET, FILM COATED in 1 BOTTLE (71335-1002-2)
ndc11
7133510023
30 TABLET, FILM COATED in 1 BOTTLE (71335-1002-3)
ndc11
7133510024
90 TABLET, FILM COATED in 1 BOTTLE (71335-1002-4)
ndc11
7133510025
120 TABLET, FILM COATED in 1 BOTTLE (71335-1002-5)
ndc11
7133510026
100 TABLET, FILM COATED in 1 BOTTLE (71335-1002-6)
ndc11
7133510027
45 TABLET, FILM COATED in 1 BOTTLE (71335-1002-7)
ndc11
7133510028
180 TABLET, FILM COATED in 1 BOTTLE (71335-1002-8)

Annotations

UNII (FDA Substance ID)

5U85DBW7LO

ESCITALOPRAM OXALATE

RxCUI 353108

Orange Book

A202389

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": {
    "43eb9e4f-1a46-46f7-9e9d-43e866963b37": {
      "match": "brand_token",
      "title": "ESCITALOPRAM TABLET, FILM COATED [BRYANT RANCH PREPACK]",
      "spl_version": "104",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1002_aa0ac792-8761-4f81-b6a4-79239182c731",
  "productndc": "71335-1002",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "202389",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE",
        "product_no": "001",
        "approval_date": "Sep 11, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "002",
        "approval_date": "Sep 11, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "003",
        "approval_date": "Sep 11, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ESCITALOPRAM OXALATE",
  "proprietary_name": "Escitalopram",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202389",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Escitalopram",
  "start_marketing_date": "20130321",
  "active_numerator_strength": "20"
}

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