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United States · US · US:68071-3357_3880e5dd-0433-2990-e063-6394a90a0ef8
Citalopram
Orange BookUNIISPLATC N06AB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeN06AB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc11680713357115 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1)
- ndc11680713357330 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3)
- ndc11680713357440 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4)
- ndc11680713357545 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5)
- ndc11680713357660 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6)
- ndc11680713357990 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9)
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": "68071-3357_3880e5dd-0433-2990-e063-6394a90a0ef8",
"productndc": "68071-3357",
"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": "40"
}Related drugs
Other records sharing ATC code N06AB04.
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