NDC 63323-315

Ganciclovir 500 mg per 10 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
Ganciclovir: every company that makes it
Form
injection, powder, lyophilized, for solution, intravenous
Strength
500 mg per 10 mL
Approval
ANDA ANDA090658
On the market since
Jun 28, 2010
Package NDCs
63323-315-41 63323-315-94
Official label
DailyMed (National Library of Medicine), updated Jan 9, 2026

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