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United States · US · US:60687-470_40d407c3-846c-cbe7-e063-6294a90a2a81

Paliperidone

Orange BookUNIISPLATC N05AX13

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAmerican Health Packaging
CountryUS (United States)
ATC codeN05AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6068747001
    100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-470-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-470-11)

Annotations

UNII (FDA Substance ID)
838F01T721
PALIPERIDONE
RxCUI 679314
Orange Book
A205618
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "838F01T721",
    "rxcui": "679314",
    "inchikey": "PMXMIIMHBWHSKN-UHFFFAOYSA-N",
    "display_name": "PALIPERIDONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f75e884e-1883-45d7-ac9b-4a6c63f2185e": {
      "match": "brand_token",
      "title": "PALIPERIDONE TABLET, EXTENDED RELEASE [BRYANT RANCH PREPACK]",
      "spl_version": "100",
      "published_date": "2026-05-28"
    }
  },
  "productid": "60687-470_40d407c3-846c-cbe7-e063-6294a90a2a81",
  "productndc": "60687-470",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "205618",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1.5MG",
        "product_no": "001",
        "approval_date": "Apr 6, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "3MG",
        "product_no": "002",
        "approval_date": "Apr 6, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "003",
        "approval_date": "Apr 6, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "9MG",
        "product_no": "004",
        "approval_date": "Apr 6, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PALIPERIDONE",
  "proprietary_name": "Paliperidone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205618",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Paliperidone",
  "start_marketing_date": "20200115",
  "active_numerator_strength": "6"
}

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