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United States · US · US:71335-2232_ff4ddb77-91cf-4e45-b855-55e4c264d085
Citalopram
Orange BookUNIISPLATC N06AB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc11713352232130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)
- ndc11713352232240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)
- ndc11713352232360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)
- ndc11713352232490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)
- ndc117133522325100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)
- ndc117133522326180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)
Annotations
UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
A077042
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": "71335-2232_ff4ddb77-91cf-4e45-b855-55e4c264d085",
"productndc": "71335-2232",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "077042",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "001",
"approval_date": "Nov 5, 2004"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 20MG BASE",
"product_no": "002",
"approval_date": "Nov 5, 2004"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 40MG BASE",
"product_no": "003",
"approval_date": "Nov 5, 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": "ANDA077042",
"marketing_category": "ANDA",
"nonproprietary_name": "citalopram",
"start_marketing_date": "20080728",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code N06AB04.
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