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United States · US · US:0456-4020_0eee9751-8886-474c-a806-8003e90cb151

Celexa

Orange BookUNIISPLATC N06AB04

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

Identification

ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeN06AB04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0456402001
    100 TABLET, FILM COATED in 1 BOTTLE (0456-4020-01)

Annotations

UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
N020822
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "I1E9D14F36",
    "rxcui": "221078",
    "inchikey": "WIHMBLDNRMIGDW-UHFFFAOYSA-N",
    "display_name": "CITALOPRAM HYDROBROMIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4259d9b1-de34-43a4-85a8-41dd214e9177": {
      "match": "brand_token",
      "title": "CELEXA (CITALOPRAM) TABLET, FILM COATED [ALLERGAN, INC.]",
      "spl_version": "39",
      "published_date": "2024-06-28"
    }
  },
  "productid": "0456-4020_0eee9751-8886-474c-a806-8003e90cb151",
  "productndc": "0456-4020",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "020822",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Apr 27, 2000"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Jul 17, 1998"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "003",
        "approval_date": "Jul 17, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 60MG BASE",
        "product_no": "004",
        "approval_date": "Jul 17, 1998"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CITALOPRAM HYDROBROMIDE",
  "proprietary_name": "Celexa",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA020822",
  "marketing_category": "NDA",
  "nonproprietary_name": "citalopram",
  "start_marketing_date": "19980717",
  "active_numerator_strength": "20"
}

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