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United States · US · US:65862-248_a8ce07ef-c51d-4af2-bafb-b0a32c090431

Escitalopram Oxalate

Orange BookUNIISPLATC N06AB10

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

Identification

ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC codeN06AB10
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6586224824
    240 mL in 1 BOTTLE (65862-248-24)

Annotations

UNII (FDA Substance ID)
5U85DBW7LO
ESCITALOPRAM OXALATE
RxCUI 353108
Orange Book
A079062
AA
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": "65862-248_a8ce07ef-c51d-4af2-bafb-b0a32c090431",
  "productndc": "65862-248",
  "dosage_form": "SOLUTION",
  "orange_book": {
    "appl_no": "079062",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "EQ 5MG BASE/5ML",
        "product_no": "001",
        "approval_date": "Apr 2, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ESCITALOPRAM OXALATE",
  "proprietary_name": "Escitalopram Oxalate",
  "active_ingred_unit": "mg/5mL",
  "application_number": "ANDA079062",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Escitalopram Oxalate",
  "start_marketing_date": "20120403",
  "active_numerator_strength": "5"
}

Related drugs

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