NDC 63323-192

Fludarabine 25 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 Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Product details

Generic drug
Fludarabine: every company that makes it
Form
injection, solution, intravenous
Strength
25 mg per 1 mL
Approval
ANDA ANDA078393
On the market since
Nov 16, 2007
Package NDCs
63323-192-02
Official label
DailyMed (National Library of Medicine), updated Oct 14, 2024

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?