# propofol

NDC: 23155-345
Generic name: propofol
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAVENOUS
Marketing started: 20211012

FDA application: ANDA206408

## 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:"23155-345"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-345
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10272dc1-657d-4798-a34a-b6341b92e560