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United States · US · US:51655-445_490edb25-d3c2-8b45-e063-6394a90a9bc2
Clonidine hydrochloride
UNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNorthwind Health Company, LLC
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc115165544518180 TABLET in 1 BOTTLE, PLASTIC (51655-445-18)
- ndc11516554452560 TABLET in 1 BOTTLE, PLASTIC (51655-445-25)
- ndc11516554452690 TABLET in 1 BOTTLE, PLASTIC (51655-445-26)
- ndc11516554455230 TABLET in 1 BOTTLE, PLASTIC (51655-445-52)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "W76I6XXF06",
"rxcui": "142432",
"inchikey": "ZNIFSRGNXRYGHF-UHFFFAOYSA-N",
"display_name": "CLONIDINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"ea1527a5-4939-4ff7-a827-f88a9113a07d": {
"match": "brand_token",
"title": "CLONIDINE HYDROCHLORIDE TABLET [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "15",
"published_date": "2026-05-28"
}
},
"productid": "51655-445_490edb25-d3c2-8b45-e063-6394a90a9bc2",
"productndc": "51655-445",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLONIDINE HYDROCHLORIDE",
"proprietary_name": "Clonidine hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA070925",
"marketing_category": "ANDA",
"nonproprietary_name": "Clonidine hydrochloride",
"start_marketing_date": "20201001",
"active_numerator_strength": ".1"
}Related drugs
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- IECatapres Ampoules 150 micrograms in 1 ml Solution for InjectionGlenwood GmbH
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