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United States · US · US:43063-925_52ba35ef-e69a-ca6e-e063-6394a90af9dd
clonidine hydrochloride
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11430639253030 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
Orange Book
A078895
ABABAB
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": "43063-925_52ba35ef-e69a-ca6e-e063-6394a90af9dd",
"productndc": "43063-925",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "078895",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.1MG",
"product_no": "001",
"approval_date": "Aug 26, 2009"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.2MG",
"product_no": "002",
"approval_date": "Aug 26, 2009"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "0.3MG",
"product_no": "003",
"approval_date": "Aug 26, 2009"
}
],
"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": "ANDA078895",
"marketing_category": "ANDA",
"nonproprietary_name": "clonidine hydrochloride",
"start_marketing_date": "20090921",
"active_numerator_strength": ".2"
}Related drugs
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