CITALOPRAM HYDROBROMIDE

Orange BookUNIISPLATC N06AB04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerExelan Pharmaceuticals Inc.

CountryUS (United States)

ATC codeN06AB04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
7628220805
500 TABLET in 1 BOTTLE (76282-208-05)
ndc11
7628220810
1000 TABLET in 1 BOTTLE (76282-208-10)
ndc11
7628220830
30 TABLET in 1 BOTTLE (76282-208-30)
ndc11
7628220890
90 TABLET in 1 BOTTLE (76282-208-90)

Annotations

UNII (FDA Substance ID)

I1E9D14F36

CITALOPRAM HYDROBROMIDE

RxCUI 221078

Orange Book

A077534

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": "76282-208_fd69f24e-8108-4b9e-92ca-13ebbdf86e45",
  "productndc": "76282-208",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077534",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Oct 3, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Oct 3, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "003",
        "approval_date": "Oct 3, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CITALOPRAM HYDROBROMIDE",
  "proprietary_name": "CITALOPRAM HYDROBROMIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077534",
  "marketing_category": "ANDA",
  "nonproprietary_name": "CITALOPRAM",
  "start_marketing_date": "20121001",
  "active_numerator_strength": "40"
}

Related drugs

Other records sharing ATC code N06AB04.

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