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United States · US · US:83270-003_4b14107a-95d4-0f90-e063-6394a90a0eb3

Methohexital Sodium

Orange BookUNIISPLATC N01AF01

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

Identification

ManufacturerONESOURCE SPECIALTY PHARMA LIMITED
CountryUS (United States)
ATC codeN01AF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8327000301
    500 mg in 1 VIAL (83270-003-01)

Annotations

UNII (FDA Substance ID)
60200PNZ7Q
METHOHEXITAL SODIUM
RxCUI 91185
Orange Book
A215488
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "60200PNZ7Q",
    "rxcui": "91185",
    "inchikey": "KDXZREBVGAGZHS-UHFFFAOYSA-M",
    "display_name": "METHOHEXITAL SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "6fb09acf-4937-47a0-a9da-084ec062da6f": {
      "match": "brand_token",
      "title": "METHOHEXITAL SODIUM INJECTION [ONESOURCE SPECIALTY PHARMA LIMITED]",
      "spl_version": "5",
      "published_date": "2026-02-23"
    }
  },
  "productid": "83270-003_4b14107a-95d4-0f90-e063-6394a90a0eb3",
  "productndc": "83270-003",
  "dosage_form": "INJECTION",
  "orange_book": {
    "appl_no": "215488",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "500MG/VIAL",
        "product_no": "001",
        "approval_date": "Oct 3, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHOHEXITAL SODIUM",
  "proprietary_name": "Methohexital Sodium",
  "active_ingred_unit": "mg/500mg",
  "application_number": "ANDA215488",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Methohexital Sodium",
  "start_marketing_date": "20260124",
  "active_numerator_strength": "500"
}

Related drugs

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