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United States · US · US:68001-237_42c4b1f4-a2c5-e21f-e063-6294a90aa481
Clonidine Hydrochloride
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBluePoint Laboratories
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116800123700100 TABLET in 1 BOTTLE (68001-237-00)
- ndc116800123703500 TABLET in 1 BOTTLE (68001-237-03)
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": "68001-237_42c4b1f4-a2c5-e21f-e063-6294a90aa481",
"productndc": "68001-237",
"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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