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United States · US · US:76420-283_e8c7a94e-8d26-886a-e053-2995a90a1ad8
Clonidine hydrochloride
UNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc117642028301100 TABLET in 1 BOTTLE (76420-283-01)
- ndc11764202832020 TABLET in 1 BOTTLE (76420-283-20)
- ndc11764202833030 TABLET in 1 BOTTLE (76420-283-30)
- ndc11764202836060 TABLET in 1 BOTTLE (76420-283-60)
- ndc11764202839090 TABLET in 1 BOTTLE (76420-283-90)
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": "76420-283_e8c7a94e-8d26-886a-e053-2995a90a1ad8",
"productndc": "76420-283",
"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": "20170601",
"active_numerator_strength": ".1"
}Related drugs
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