NDC 63323-738

Famotidine 10 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
Famotidine: every company that makes it
Form
injection, solution, intravenous
Strength
10 mg per 1 mL
Approval
ANDA ANDA075709
On the market since
Jul 19, 2001
Package NDCs
63323-738-03 63323-738-06 63323-738-09 63323-738-20
Official label
DailyMed (National Library of Medicine), updated Oct 20, 2022

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