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United States · US · US:50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78
Pramipexole Dihydrochloride
Orange BookUNIISPLATC N04BC05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeN04BC05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500903280090 TABLET in 1 BOTTLE (50090-3280-0)
Annotations
UNII (FDA Substance ID)
3D867NP06J
PRAMIPEXOLE DIHYDROCHLORIDE
RxCUI 236747
Orange Book
A202633
ABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3D867NP06J",
"rxcui": "236747",
"inchikey": "APVQOOKHDZVJEX-QTPLPEIMSA-N",
"display_name": "PRAMIPEXOLE DIHYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"46f88017-7b0e-437e-90b1-37bdf9013e72": {
"match": "brand_token",
"title": "PRAMIPEXOLE DIHYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]",
"spl_version": "104",
"published_date": "2026-05-25"
}
},
"productid": "50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78",
"productndc": "50090-3280",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "202633",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.125MG",
"product_no": "001",
"approval_date": "Oct 26, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "002",
"approval_date": "Oct 26, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.5MG",
"product_no": "003",
"approval_date": "Oct 26, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.75MG",
"product_no": "004",
"approval_date": "Oct 26, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "005",
"approval_date": "Oct 26, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1.5MG",
"product_no": "006",
"approval_date": "Oct 26, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PRAMIPEXOLE DIHYDROCHLORIDE",
"proprietary_name": "Pramipexole Dihydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202633",
"marketing_category": "ANDA",
"nonproprietary_name": "Pramipexole Dihydrochloride",
"start_marketing_date": "20121026",
"active_numerator_strength": ".25"
}Related drugs
Other records sharing ATC code N04BC05.
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