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United States · US · US:62135-939_2e81bd7d-c434-2d02-e063-6294a90a196d
Thioridazine Hydrochloride
Orange BookUNIISPLATC N05AC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerChartwell RX, LLC
CountryUS (United States)
ATC codeN05AC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11621359399090 TABLET, FILM COATED in 1 BOTTLE (62135-939-90)
Annotations
UNII (FDA Substance ID)
4WCI67NK8M
THIORIDAZINE HYDROCHLORIDE
RxCUI 203165
Orange Book
A088135
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4WCI67NK8M",
"rxcui": "203165",
"inchikey": "NZFNXWQNBYZDAQ-UHFFFAOYSA-N",
"display_name": "THIORIDAZINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"1fd16a99-e856-4a37-9dae-c443714fac14": {
"match": "brand_token",
"title": "THIORIDAZINE HYDROCHLORIDE TABLET, FILM COATED [SAFECOR HEALTH LLC]",
"spl_version": "2",
"published_date": "2026-03-04"
}
},
"productid": "62135-939_2e81bd7d-c434-2d02-e063-6294a90a196d",
"productndc": "62135-939",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "088135",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "100MG",
"product_no": "001",
"approval_date": "Nov 20, 1984"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "THIORIDAZINE HYDROCHLORIDE",
"proprietary_name": "Thioridazine Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA088135",
"marketing_category": "ANDA",
"nonproprietary_name": "Thioridazine Hydrochloride",
"start_marketing_date": "19841120",
"active_numerator_strength": "100"
}Related drugs
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