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For Regional Anesthesia. ANDA 77908, held by Hospira. Propofol.
As of Nov 14, 2026, ANDA 77908 (Propofol), held by Hospira, was first approved by FDA on Mar 17, 2006, with 6 approved supplements and 0 published complete response letters.
First approved: Mar 17, 2006
Supplements approved: 6
Complete response letters: 0
What It's For
From the FDA-approved label (Indications and Usage)
Propofol injectable emulsion is an intravenous general anesthetic and sedation drug indicated for:
Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of Age
Maintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of Age
Initiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult Patients
Sedation for Adult Patients in Combination with Regional Anesthesia
Intensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult Patients Limitations of Use Propofol injectable emulsion is not recommended for induction of anesthesia below the age of 3 years or for maintenance of anesthesia below the age of 2 m…
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters.Drugs@FDA and FDA complete response letters
