Loxapine

Orange BookUNIISPLATC N05AH01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerREMEDYREPACK INC.

CountryUS (United States)

ATC codeN05AH01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7051818960
30 CAPSULE in 1 BLISTER PACK (70518-1896-0)

Annotations

UNII (FDA Substance ID)

X59SG0MRYU

LOXAPINE SUCCINATE

RxCUI 6476

Orange Book

A090695

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "X59SG0MRYU",
    "rxcui": "6476",
    "inchikey": "YQZBAXDVDZTKEQ-UHFFFAOYSA-N",
    "display_name": "LOXAPINE SUCCINATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ae8e299c-4003-4ccf-badc-fb665a997b20": {
      "match": "brand_token",
      "title": "LOXAPINE CAPSULE [REMEDYREPACK INC.]",
      "spl_version": "18",
      "published_date": "2026-02-19"
    }
  },
  "productid": "70518-1896_498785a0-8e91-16f9-e063-6394a90ac352",
  "productndc": "70518-1896",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "090695",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE",
        "product_no": "001",
        "approval_date": "Sep 26, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "002",
        "approval_date": "Sep 26, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "003",
        "approval_date": "Sep 26, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "004",
        "approval_date": "Sep 26, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LOXAPINE SUCCINATE",
  "proprietary_name": "Loxapine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090695",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Loxapine",
  "start_marketing_date": "20190221",
  "active_numerator_strength": "25"
}

Related drugs

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