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United States · US · US:16729-238_23980eef-2eb5-2b74-e063-6394a90a68ac
ropinirole
Orange BookUNIISPLATC N04BC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAccord Healthcare Inc.
CountryUS (United States)
ATC codeN04BC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc111672923801100 TABLET, FILM COATED in 1 BOTTLE (16729-238-01)
Annotations
UNII (FDA Substance ID)
D7ZD41RZI9
ROPINIROLE HYDROCHLORIDE
RxCUI 236553
Orange Book
A204022
ABABABABABABAB
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": "16729-238_23980eef-2eb5-2b74-e063-6394a90a68ac",
"productndc": "16729-238",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "204022",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 0.25MG BASE",
"product_no": "001",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 0.5MG BASE",
"product_no": "002",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 1MG BASE",
"product_no": "003",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2MG BASE",
"product_no": "004",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 3MG BASE",
"product_no": "005",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 4MG BASE",
"product_no": "006",
"approval_date": "Feb 28, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 5MG BASE",
"product_no": "007",
"approval_date": "Feb 28, 2017"
}
],
"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": "ANDA204022",
"marketing_category": "ANDA",
"nonproprietary_name": "ropinirole",
"start_marketing_date": "20181017",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N04BC04.
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