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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

  • ndc11
    6838211301
    100 TABLET, FILM COATED in 1 BOTTLE (68382-113-01)
  • ndc11
    6838211305
    500 TABLET, FILM COATED in 1 BOTTLE (68382-113-05)
  • ndc11
    6838211306
    30 TABLET, FILM COATED in 1 BOTTLE (68382-113-06)
  • ndc11
    6838211310
    1000 TABLET, FILM COATED in 1 BOTTLE (68382-113-10)
  • ndc11
    6838211314
    60 TABLET, FILM COATED in 1 BOTTLE (68382-113-14)
  • ndc11
    6838211316
    90 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"
}

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