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United States · US · US:42806-021_b7f54932-2c8c-44f4-acc6-d9e2b3914be9

CITALOPRAM

Orange BookUNIISPLATC N06AB04

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

Identification

ManufacturerEpic Pharma, LLC
CountryUS (United States)
ATC codeN06AB04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    4280602101
    100 TABLET, FILM COATED in 1 BOTTLE (42806-021-01)
  • ndc11
    4280602110
    1000 TABLET, FILM COATED in 1 BOTTLE (42806-021-10)
  • ndc11
    4280602130
    30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)

Annotations

UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
A077045
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": {
    "df8db06a-ced7-4dd6-83bd-c61d2f68f1b1": {
      "match": "brand_token",
      "title": "CITALOPRAM TABLET, FILM COATED [ASCLEMED USA INC.]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "42806-021_b7f54932-2c8c-44f4-acc6-d9e2b3914be9",
  "productndc": "42806-021",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077045",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "001",
        "approval_date": "Apr 29, 2005"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Apr 29, 2005"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "003",
        "approval_date": "Apr 29, 2005"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CITALOPRAM HYDROBROMIDE",
  "proprietary_name": "CITALOPRAM",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077045",
  "marketing_category": "ANDA",
  "nonproprietary_name": "citalopram",
  "start_marketing_date": "20110520",
  "active_numerator_strength": "40"
}

Related drugs

Other records sharing ATC code N06AB04.

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