NDC 63323-342

Cefoxitin 2 g powder, for solution

On the label: Fresenius Kabi, LLC.

Italy: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ACS Dobfar SpAVerona, ItalyMakes it, tests it and packages it Problems found, fixed voluntarilyOct 27, 2023 · 6 inspections

Product details

Generic drug
Cefoxitin: every company that makes it
Form
powder, for solution, intravenous
Strength
2 g
Approval
ANDA ANDA065414
On the market since
Jul 6, 2011
Package NDCs
63323-342-29 63323-342-41
Official label
DailyMed (National Library of Medicine), updated Jul 10, 2023

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