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United States · US · US:71335-1893_8a7f725b-ad42-4dfc-97df-ac900509f7b0
Aripiprazole
Orange BookUNIISPLATC N05AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc11713351893130 TABLET in 1 BOTTLE (71335-1893-1)
- ndc11713351893228 TABLET in 1 BOTTLE (71335-1893-2)
- ndc11713351893390 TABLET in 1 BOTTLE (71335-1893-3)
- ndc11713351893460 TABLET in 1 BOTTLE (71335-1893-4)
- ndc117133518935120 TABLET in 1 BOTTLE (71335-1893-5)
- ndc11713351893615 TABLET in 1 BOTTLE (71335-1893-6)
Annotations
UNII (FDA Substance ID)
82VFR53I78
ARIPIPRAZOLE
RxCUI 89013
Orange Book
A205064
ABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "82VFR53I78",
"rxcui": "89013",
"inchikey": "CEUORZQYGODEFX-UHFFFAOYSA-N",
"display_name": "ARIPIPRAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"52cc86ba-2c4f-1aba-e063-6294a90a844e": {
"match": "brand_token",
"title": "ARIPIPRAZOLE TABLET [COUPLER LLC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "71335-1893_8a7f725b-ad42-4dfc-97df-ac900509f7b0",
"productndc": "71335-1893",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "205064",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "001",
"approval_date": "Apr 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "002",
"approval_date": "Apr 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "003",
"approval_date": "Apr 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "004",
"approval_date": "Apr 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "005",
"approval_date": "Apr 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "006",
"approval_date": "Apr 28, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ARIPIPRAZOLE",
"proprietary_name": "Aripiprazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA205064",
"marketing_category": "ANDA",
"nonproprietary_name": "Aripiprazole",
"start_marketing_date": "20150428",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N05AX12.
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