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United States · US · US:37662-0342_e0cc472a-dbac-71c3-e053-2995a90adf50
Citalopram
UNIISPLATC N06AB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeN06AB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766203421200 PELLET in 1 VIAL, GLASS (37662-0342-1)
- ndc113766203422500 PELLET in 1 VIAL, GLASS (37662-0342-2)
- ndc1137662034233000 PELLET in 1 BOTTLE, GLASS (37662-0342-3)
- ndc11376620342410000 PELLET in 1 BOTTLE, GLASS (37662-0342-4)
Annotations
UNII (FDA Substance ID)
0DHU5B8D6V
CITALOPRAM
RxCUI 2556
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0DHU5B8D6V",
"rxcui": "2556",
"inchikey": "WSEQXVZVJXJVFP-UHFFFAOYSA-N",
"display_name": "CITALOPRAM",
"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": "37662-0342_e0cc472a-dbac-71c3-e053-2995a90adf50",
"productndc": "37662-0342",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CITALOPRAM",
"proprietary_name": "Citalopram",
"active_ingred_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Citalopram",
"start_marketing_date": "20220606",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code N06AB04.
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