# Sevoflurane

NDC: 0781-6160
Generic name: Sevoflurane
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: RESPIRATORY (INHALATION)
Marketing started: 20170125

FDA application: ANDA203793

## Active ingredients

- SEVOFLURANE: 250 mL/250mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-6160"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-6160
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8604f245-fa99-4092-9042-058aa42e0b74