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United States · US · US:68071-4661_2bed1bae-519d-1bb9-e063-6294a90a795b
Clonidine Hydrochloride
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116807146612120 TABLET in 1 BOTTLE (68071-4661-2)
- ndc11680714661990 TABLET in 1 BOTTLE (68071-4661-9)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
Orange Book
A070974
AB
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": "68071-4661_2bed1bae-519d-1bb9-e063-6294a90a795b",
"productndc": "68071-4661",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070974",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.1MG",
"product_no": "001",
"approval_date": "Dec 16, 1986"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLONIDINE HYDROCHLORIDE",
"proprietary_name": "Clonidine Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA070974",
"marketing_category": "ANDA",
"nonproprietary_name": "Clonidine Hydrochloride",
"start_marketing_date": "19950103",
"active_numerator_strength": ".1"
}Related drugs
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Access this data programmatically
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