NDC 18124-011

Cleviprex 0.5 mg per 1 mL emulsion

On the label: Fresenius Kabi Austria GmbH.

Austria: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi Austria GmbHLinz, AustriaMakes it and makes the active ingredient Problems found, fixed voluntarilyMay 23, 2025 · 6 inspections

Product details

Generic drug
Clevidipine: every company that makes it
Form
emulsion, intravenous
Strength
0.5 mg per 1 mL
Approval
NDA NDA022156
On the market since
Sep 15, 2008
Package NDCs
18124-011-00 18124-011-25 18124-011-50
Official label
DailyMed (National Library of Medicine), updated Nov 9, 2022

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