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United States · US · US:71335-0777_bc883971-73e7-43b2-8b10-840c87eaa79e
clonidine hydrochloride
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc11713350777024 TABLET in 1 BOTTLE (71335-0777-0)
- ndc117133507771100 TABLET in 1 BOTTLE (71335-0777-1)
- ndc11713350777230 TABLET in 1 BOTTLE (71335-0777-2)
- ndc11713350777320 TABLET in 1 BOTTLE (71335-0777-3)
- ndc11713350777460 TABLET in 1 BOTTLE (71335-0777-4)
- ndc117133507775120 TABLET in 1 BOTTLE (71335-0777-5)
- ndc11713350777690 TABLET in 1 BOTTLE (71335-0777-6)
- ndc11713350777710 TABLET in 1 BOTTLE (71335-0777-7)
- ndc11713350777845 TABLET in 1 BOTTLE (71335-0777-8)
- ndc11713350777914 TABLET in 1 BOTTLE (71335-0777-9)
Annotations
UNII (FDA Substance ID)
W76I6XXF06
CLONIDINE HYDROCHLORIDE
RxCUI 142432
Orange Book
A091368
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": "71335-0777_bc883971-73e7-43b2-8b10-840c87eaa79e",
"productndc": "71335-0777",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "091368",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.1MG",
"product_no": "001",
"approval_date": "Dec 6, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.2MG",
"product_no": "002",
"approval_date": "Dec 6, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.3MG",
"product_no": "003",
"approval_date": "Dec 6, 2011"
}
],
"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": "ANDA091368",
"marketing_category": "ANDA",
"nonproprietary_name": "Clonidine Hydrochloride",
"start_marketing_date": "20160503",
"active_numerator_strength": ".1"
}Related drugs
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