# Propofol Injectable Emulsion

NDC: 43598-548
Generic name: Propofol Injectable Emulsion
Labeler / Manufacturer: Dr. Reddy's Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAVENOUS
Marketing started: 20181115

FDA application: ANDA205067

## 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:"43598-548"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-548
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=800646b8-83a8-01d9-3dc8-bb2ddcb8570c