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United States · US · US:43063-063_2b24d618-2b9f-f54e-e063-6394a90a9c46

Citalopram

Orange BookUNIISPLATC N06AB04

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

Identification

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

Packs · 4

  • ndc11
    4306306314
    14 TABLET in 1 BOTTLE, PLASTIC (43063-063-14)
  • ndc11
    4306306330
    30 TABLET in 1 BOTTLE, PLASTIC (43063-063-30)
  • ndc11
    4306306360
    60 TABLET in 1 BOTTLE, PLASTIC (43063-063-60)
  • ndc11
    4306306390
    90 TABLET in 1 BOTTLE, PLASTIC (43063-063-90)

Annotations

UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
A077289
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": "43063-063_2b24d618-2b9f-f54e-e063-6394a90a9c46",
  "productndc": "43063-063",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077289",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Nov 30, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Nov 30, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 40MG BASE",
        "product_no": "003",
        "approval_date": "Nov 30, 2006"
      }
    ],
    "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": "ANDA077289",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Citalopram",
  "start_marketing_date": "20100406",
  "active_numerator_strength": "20"
}

Related drugs

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