# Methohexital Sodium

NDC: 23155-893
Generic name: Methohexital Sodium
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, RECTAL
Marketing started: 20241212

FDA application: ANDA215488

## Active ingredients

- METHOHEXITAL SODIUM: 500 mg/500mg

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-893"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-893
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f76d4ab9-2f6c-420b-afec-b9cdfdc083ce