Citalopram

Orange BookUNIISPLATC N06AB04

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

Identification

ManufacturerAurobindo Pharma Limited

CountryUS (United States)

ATC codeN06AB04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
6586200601
100 TABLET, FILM COATED in 1 BOTTLE (65862-006-01)
ndc11
6586200605
500 TABLET, FILM COATED in 1 BOTTLE (65862-006-05)
ndc11
6586200610
10 BLISTER PACK in 1 CARTON (65862-006-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
ndc11
6586200630
30 TABLET, FILM COATED in 1 BOTTLE (65862-006-30)
ndc11
6586200632
30 TABLET, FILM COATED in 1 BLISTER PACK (65862-006-32)
ndc11
6586200660
60 TABLET, FILM COATED in 1 BOTTLE (65862-006-60)
ndc11
6586200690
90 TABLET, FILM COATED in 1 BOTTLE (65862-006-90)

Annotations

UNII (FDA Substance ID)

I1E9D14F36

CITALOPRAM HYDROBROMIDE

RxCUI 221078

Orange Book

A077031

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": "65862-006_5642ea11-17b4-431a-a896-2cb336929100",
  "productndc": "65862-006",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077031",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Oct 28, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Oct 28, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "003",
        "approval_date": "Oct 28, 2004"
      }
    ],
    "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": "ANDA077031",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Citalopram Hydrobromide",
  "start_marketing_date": "20041028",
  "active_numerator_strength": "20"
}

Related drugs

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