# Methohexital Sodium

NDC: 83270-003
Generic name: Methohexital Sodium
Labeler / Manufacturer: ONESOURCE SPECIALTY PHARMA LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260124

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:"83270-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83270-003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fb09acf-4937-47a0-a9da-084ec062da6f