NDC 63323-104

Etoposide 20 mg per 1 mL injection, solution

On the label: Fresenius Kabi, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
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
Etoposide: every company that makes it
Form
injection, solution, intravenous
Strength
20 mg per 1 mL
Approval
ANDA ANDA074983
On the market since
Jul 18, 2001
Package NDCs
63323-104-01 63323-104-05 63323-104-06 63323-104-25 63323-104-50
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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