NDC 51662-1470

Propofol 10 mg per 1 mL injection, emulsion

On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-4699.

India: 1

Where the pills inside were 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

Repackaging site

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
Dec 14, 2019
Package NDCs
51662-1470-1
Official label
DailyMed (National Library of Medicine), updated Jan 8, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?