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United States · US · US:71511-503_4f83c93a-721f-ca2f-e063-6394a90aa789
Nexiclon XR
Orange BookUNIISPLATC C02AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRosemont Pharmaceuticals LLC
CountryUS (United States)
ATC codeC02AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11715115033030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71511-503-30)
Annotations
UNII (FDA Substance ID)
MN3L5RMN02
CLONIDINE
RxCUI 2599
Orange Book
N022500
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "MN3L5RMN02",
"rxcui": "2599",
"inchikey": "GJSURZIOUXUGAL-UHFFFAOYSA-N",
"display_name": "CLONIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"dad35a6f-d57e-f302-e053-2995a90a9efb": {
"match": "brand_token",
"title": "NEXICLON XR (CLONIDINE) TABLET, EXTENDED RELEASE [ROSEMONT PHARMACEUTICALS LLC]",
"spl_version": "2",
"published_date": "2026-04-17"
}
},
"productid": "71511-503_4f83c93a-721f-ca2f-e063-6394a90aa789",
"productndc": "71511-503",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "022500",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 0.17MG BASE",
"product_no": "001",
"approval_date": "Dec 3, 2009"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 0.26MG BASE",
"product_no": "002",
"approval_date": "Dec 3, 2009"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLONIDINE",
"proprietary_name": "Nexiclon XR",
"active_ingred_unit": "mg/1",
"application_number": "NDA022500",
"marketing_category": "NDA",
"nonproprietary_name": "Clonidine",
"start_marketing_date": "20220301",
"active_numerator_strength": ".17"
}Related drugs
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Access this data programmatically
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