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United States · US · US:23155-893_9ec15df7-278e-4cf3-bc97-e480b4671ca6
Methohexital Sodium
Orange BookUNIISPLATC N01AF01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN01AF01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1123155893311 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL
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": "INTRAMUSCULAR; INTRAVENOUS; RECTAL",
"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": "23155-893_9ec15df7-278e-4cf3-bc97-e480b4671ca6",
"productndc": "23155-893",
"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": "20241212",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code N01AF01.
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