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Methohexital Sodium

NDC 23155-893 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215488
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS RECTAL
Active ingredientsMETHOHEXITAL SODIUM (500 mg/500mg)
Marketing started20241212
Package count1

External sources

Source: openFDA. Public-domain (CC0).