NDC 63323-314

Vancomycin Hydrochloride 10 g per 100 mL injection, powder, lyophilized, for solution

On the label: Fresenius Kabi, LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi USA, LLCGrand Island, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action
Fresenius Kabi USA, LLCMelrose Park, IL, United StatesMakes it and tests it Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Product details

Generic drug
Vancomycin: every company that makes it
Form
injection, powder, lyophilized, for solution, intravenous
Strength
10 g per 100 mL
Approval
ANDA ANDA062663
On the market since
Nov 30, 2004
Package NDCs
63323-314-66
Official label
DailyMed (National Library of Medicine), updated Feb 7, 2023

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