escitalopram oxalate

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
7133506851
60 TABLET in 1 BOTTLE (71335-0685-1)
ndc11
7133506852
28 TABLET in 1 BOTTLE (71335-0685-2)
ndc11
7133506853
30 TABLET in 1 BOTTLE (71335-0685-3)
ndc11
7133506854
90 TABLET in 1 BOTTLE (71335-0685-4)
ndc11
7133506855
120 TABLET in 1 BOTTLE (71335-0685-5)
ndc11
7133506856
100 TABLET in 1 BOTTLE (71335-0685-6)
ndc11
7133506857
45 TABLET in 1 BOTTLE (71335-0685-7)
ndc11
7133506858
180 TABLET in 1 BOTTLE (71335-0685-8)

Annotations

UNII (FDA Substance ID)

5U85DBW7LO

ESCITALOPRAM OXALATE

RxCUI 353108

Orange Book

A090939

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": "71335-0685_7cb6e260-dd56-42fd-aaca-4cc1fd460884",
  "productndc": "71335-0685",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "090939",
    "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 oxalate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090939",
  "marketing_category": "ANDA",
  "nonproprietary_name": "escitalopram oxalate",
  "start_marketing_date": "20120911",
  "active_numerator_strength": "20"
}

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