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United States · US · US:69680-146_232ae12c-b9bc-4ca7-982e-d6f43b6c8eec
Pramipexole Dihydrochloride
Orange BookUNIISPLATC N04BC05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerVitruvias Therapeutics, Inc.
CountryUS (United States)
ATC codeN04BC05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11696801463030 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-146-30)
Annotations
UNII (FDA Substance ID)
3D867NP06J
PRAMIPEXOLE DIHYDROCHLORIDE
RxCUI 236747
Orange Book
A212797
ABAB
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": "69680-146_232ae12c-b9bc-4ca7-982e-d6f43b6c8eec",
"productndc": "69680-146",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "212797",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.375MG",
"product_no": "001",
"approval_date": "Jun 11, 2021"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.75MG",
"product_no": "002",
"approval_date": "Jun 11, 2021"
}
],
"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": "ANDA212797",
"marketing_category": "ANDA",
"nonproprietary_name": "Pramipexole Dihydrochloride",
"start_marketing_date": "20210827",
"active_numerator_strength": ".75"
}Related drugs
Other records sharing ATC code N04BC05.
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