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United States · US · US:43063-908_32d6d5a1-fa47-3097-e063-6294a90ac4e0
RISPERIDONE
Orange BookUNIISPLATC N05AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN05AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1143063908077 TABLET in 1 BOTTLE, PLASTIC (43063-908-07)
- ndc11430639083030 TABLET in 1 BOTTLE, PLASTIC (43063-908-30)
- ndc11430639086060 TABLET in 1 BOTTLE, PLASTIC (43063-908-60)
Annotations
UNII (FDA Substance ID)
L6UH7ZF8HC
RISPERIDONE
RxCUI 35636
Orange Book
A201003
ABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "L6UH7ZF8HC",
"rxcui": "35636",
"inchikey": "RAPZEAPATHNIPO-UHFFFAOYSA-N",
"display_name": "RISPERIDONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"43aa2a4f-1123-4f86-800b-9218882f7bcd": {
"match": "brand_token",
"title": "RISPERIDONE TABLET [SOLCO HEALTHCARE US, LLC]",
"spl_version": "14",
"published_date": "2026-05-26"
}
},
"productid": "43063-908_32d6d5a1-fa47-3097-e063-6294a90ac4e0",
"productndc": "43063-908",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "201003",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "001",
"approval_date": "Aug 24, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.5MG",
"product_no": "002",
"approval_date": "Aug 24, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "003",
"approval_date": "Aug 24, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "004",
"approval_date": "Aug 24, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3MG",
"product_no": "005",
"approval_date": "Aug 24, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "4MG",
"product_no": "006",
"approval_date": "Aug 24, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RISPERIDONE",
"proprietary_name": "RISPERIDONE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA201003",
"marketing_category": "ANDA",
"nonproprietary_name": "RISPERIDONE",
"start_marketing_date": "20140328",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code N05AX08.
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