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United States · US · US:68382-113_2af53e64-46a6-4b12-9ac8-8f8031a8bd97
risperidone
Orange BookUNIISPLATC N05AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeN05AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc116838211301100 TABLET, FILM COATED in 1 BOTTLE (68382-113-01)
- ndc116838211305500 TABLET, FILM COATED in 1 BOTTLE (68382-113-05)
- ndc11683821130630 TABLET, FILM COATED in 1 BOTTLE (68382-113-06)
- ndc1168382113101000 TABLET, FILM COATED in 1 BOTTLE (68382-113-10)
- ndc11683821131460 TABLET, FILM COATED in 1 BOTTLE (68382-113-14)
- ndc11683821131690 TABLET, FILM COATED in 1 BOTTLE (68382-113-16)
Annotations
UNII (FDA Substance ID)
L6UH7ZF8HC
RISPERIDONE
RxCUI 35636
Orange Book
A078040
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": "68382-113_2af53e64-46a6-4b12-9ac8-8f8031a8bd97",
"productndc": "68382-113",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "078040",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "001",
"approval_date": "Oct 16, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.5MG",
"product_no": "002",
"approval_date": "Oct 16, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "003",
"approval_date": "Oct 16, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "004",
"approval_date": "Oct 16, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3MG",
"product_no": "005",
"approval_date": "Oct 16, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "4MG",
"product_no": "006",
"approval_date": "Oct 16, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RISPERIDONE",
"proprietary_name": "risperidone",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078040",
"marketing_category": "ANDA",
"nonproprietary_name": "risperidone",
"start_marketing_date": "20081113",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code N05AX08.
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