# PROPOFOL

NDC: 80830-2364
Generic name: propofol
Labeler / Manufacturer: Amneal Pharmaceuticals Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAVENOUS
Marketing started: 20240816

FDA application: ANDA217525

## Active ingredients

- PROPOFOL: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80830-2364"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80830-2364
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6833edd6-ba8a-4b97-a872-ab253c64a903