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United States · US · US:17856-0564_34f3a909-1a50-3667-e063-6294a90aa4aa
Citalopram Hydrobromide
Orange BookUNIISPLATC N06AB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerATLANTIC BIOLOGICALS CORP.
CountryUS (United States)
ATC codeN06AB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11178560564172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0564-1) / 10 mL in 1 CUP, UNIT-DOSE
Annotations
UNII (FDA Substance ID)
I1E9D14F36
CITALOPRAM HYDROBROMIDE
RxCUI 221078
Orange Book
A201450
AA
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": "17856-0564_34f3a909-1a50-3667-e063-6294a90aa4aa",
"productndc": "17856-0564",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "201450",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "EQ 10MG BASE/5ML",
"product_no": "001",
"approval_date": "Dec 15, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CITALOPRAM HYDROBROMIDE",
"proprietary_name": "Citalopram Hydrobromide",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA201450",
"marketing_category": "ANDA",
"nonproprietary_name": "Citalopram Hydrobromide",
"start_marketing_date": "20190531",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code N06AB04.
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