Citalopram Hydrobromide

Orange BookUNIISPLATC N06AB04

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AB04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7133502381
30 TABLET in 1 BOTTLE (71335-0238-1)
ndc11
7133502382
60 TABLET in 1 BOTTLE (71335-0238-2)
ndc11
7133502383
90 TABLET in 1 BOTTLE (71335-0238-3)
ndc11
7133502384
100 TABLET in 1 BOTTLE (71335-0238-4)
ndc11
7133502385
15 TABLET in 1 BOTTLE (71335-0238-5)
ndc11
7133502386
120 TABLET in 1 BOTTLE (71335-0238-6)
ndc11
7133502387
7 TABLET in 1 BOTTLE (71335-0238-7)

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": "71335-0238_e98dc453-0638-4318-9778-e9a881646d36",
  "productndc": "71335-0238",
  "dosage_form": "TABLET",
  "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 Hydrobromide",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078216",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Citalopram Hydrobromide",
  "start_marketing_date": "20071018",
  "active_numerator_strength": "20"
}

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