Brevital Sodium

{
  "unii": {
    "unii": "60200PNZ7Q",
    "rxcui": "91185",
    "inchikey": "KDXZREBVGAGZHS-UHFFFAOYSA-M",
    "display_name": "METHOHEXITAL SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS; RECTAL",
  "spl_meta": {
    "eccd8340-ead3-4363-8902-0c19d33aa2ac": {
      "match": "brand_token",
      "title": "BREVITAL SODIUM (METHOHEXITAL SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [PAR HEALTH USA, LLC]",
      "spl_version": "18",
      "published_date": "2026-05-20"
    }
  },
  "productid": "42023-105_6efcbde7-9a3d-4d12-93ea-793a9e72725a",
  "productndc": "42023-105",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "orange_book": {
    "appl_no": "011559",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "500MG/VIAL",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "2.5GM/VIAL",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5GM/VIAL",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG/VIAL",
        "product_no": "004",
        "approval_date": "Dec 21, 2012"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHOHEXITAL SODIUM",
  "proprietary_name": "Brevital Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA011559",
  "marketing_category": "NDA",
  "nonproprietary_name": "methohexital sodium",
  "start_marketing_date": "20071101",
  "active_numerator_strength": "500"
}