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United States · US · US:0228-3659_3499549d-d3ad-4636-8234-2539c0fbfac1
Ropinirole
Orange BookUNIISPLATC N04BC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerActavis Pharma, Inc.
CountryUS (United States)
ATC codeN04BC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11022836590330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3659-03)
- ndc11022836590990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3659-09)
Annotations
UNII (FDA Substance ID)
D7ZD41RZI9
ROPINIROLE HYDROCHLORIDE
RxCUI 236553
Orange Book
A090869
ABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "D7ZD41RZI9",
"rxcui": "236553",
"inchikey": "XDXHAEQXIBQUEZ-UHFFFAOYSA-N",
"display_name": "ROPINIROLE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c89f68e5-d2ad-4aad-a63c-c32eff5e82c9": {
"match": "brand_token",
"title": "ROPINIROLE TABLET, FILM COATED [BRYANT RANCH PREPACK]",
"spl_version": "101",
"published_date": "2026-06-01"
}
},
"productid": "0228-3659_3499549d-d3ad-4636-8234-2539c0fbfac1",
"productndc": "0228-3659",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "090869",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2MG BASE",
"product_no": "001",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 4MG BASE",
"product_no": "002",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 6MG BASE",
"product_no": "003",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 8MG BASE",
"product_no": "004",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 12MG BASE",
"product_no": "005",
"approval_date": "May 17, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ROPINIROLE HYDROCHLORIDE",
"proprietary_name": "Ropinirole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090869",
"marketing_category": "ANDA",
"nonproprietary_name": "Ropinirole",
"start_marketing_date": "20120823",
"active_numerator_strength": "4"
}Related drugs
Other records sharing ATC code N04BC04.
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