NDC 0409-0501

Propofol 10 mg per 1 mL injection, emulsion

On the label: Hospira, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pfizer Healthcare India Private LimitedAnakapalli, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Propofol: every company that makes it
Form
injection, emulsion, intravenous
Strength
10 mg per 1 mL
Approval
ANDA ANDA077908
On the market since
Aug 17, 2026
Package NDCs
0409-0501-97 0409-0501-98
Official label
DailyMed (National Library of Medicine), updated Aug 13, 2026

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