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United States · US · US:51655-362_49dad799-16e1-cbba-e063-6294a90a720f
Clonidine Hydrochloride
Orange BookUNIISPLATC 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 · 2
- ndc11516553622690 TABLET in 1 BOTTLE, PLASTIC (51655-362-26)
- ndc11516553625230 TABLET in 1 BOTTLE, DISPENSING (51655-362-52)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
Orange Book
A070975
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": "51655-362_49dad799-16e1-cbba-e063-6294a90a720f",
"productndc": "51655-362",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070975",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.2MG",
"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": "ANDA070975",
"marketing_category": "ANDA",
"nonproprietary_name": "Clonidine Hydrochloride",
"start_marketing_date": "20140924",
"active_numerator_strength": ".2"
}Related drugs
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Access this data programmatically
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