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United States · US · US:87063-221_52ee1af5-9a84-797c-e063-6294a90ab63d

Citalopram

Orange BookUNIISPLATC N06AB04

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

Identification

ManufacturerASCLEMED USA INC.
CountryUS (United States)
ATC codeN06AB04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    8706322101
    100 TABLET, FILM COATED in 1 BOTTLE (87063-221-01)
  • ndc11
    8706322110
    10 TABLET, FILM COATED in 1 BOTTLE (87063-221-10)
  • ndc11
    8706322120
    20 TABLET, FILM COATED in 1 BOTTLE (87063-221-20)
  • ndc11
    8706322130
    30 TABLET, FILM COATED in 1 BOTTLE (87063-221-30)
  • ndc11
    8706322160
    60 TABLET, FILM COATED in 1 BOTTLE (87063-221-60)
  • ndc11
    8706322190
    90 TABLET, FILM COATED in 1 BOTTLE (87063-221-90)

Annotations

UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
A078216
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": "87063-221_52ee1af5-9a84-797c-e063-6294a90ab63d",
  "productndc": "87063-221",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078216",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Mar 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Mar 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "003",
        "approval_date": "Mar 27, 2007"
      }
    ],
    "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": "ANDA078216",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Citalopram",
  "start_marketing_date": "20071018",
  "active_numerator_strength": "40"
}

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