# SEVOFLURANE

NDC: 10019-653
Generic name: Sevoflurane
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: RESPIRATORY (INHALATION)
Marketing started: 20020707

FDA application: ANDA075895

## 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:"10019-653"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10019-653
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22700993-851a-48aa-941e-1d2b6b04081f