# Propofol

NDC: 72572-601
Generic name: Propofol
Labeler / Manufacturer: Civica, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAVENOUS
Marketing started: 20210716

FDA application: ANDA205576

## Active ingredients

- PROPOFOL: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72572-601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ba70032-40c2-41c5-9f99-d1f94032d3dc
