# Desflurane

NDC: 0781-6172
Generic name: desflurane
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: RESPIRATORY (INHALATION)
Marketing started: 20180226

FDA application: ANDA208234

## Active ingredients

- DESFLURANE: 240 mL/240mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-6172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-6172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21ba0e18-3dbc-4feb-a3a4-f6470c00910a