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United States · US · US:70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e
Clonidine Hydrochloride
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSomerset Therapeutics, LLC
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11700690440160 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
Orange Book
A211433
AB1
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": "70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e",
"productndc": "70069-044",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "211433",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "0.1MG",
"product_no": "001",
"approval_date": "Oct 12, 2018"
}
],
"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": "ANDA211433",
"marketing_category": "ANDA",
"nonproprietary_name": "Clonidine Hydrochloride",
"start_marketing_date": "20250304",
"active_numerator_strength": ".1"
}Related drugs
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