NDC 65219-257

Ephedrine Sulfate 50 mg per 1 mL injection

On the label: Fresenius Kabi USA, LLC.

United States: 1

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

Product details

Generic drug
Ephedrine: every company that makes it
Form
injection, intravenous
Strength
50 mg per 1 mL
Approval
ANDA ANDA209646
On the market since
Oct 31, 2020
Package NDCs
65219-257-00 65219-257-01
Official label
DailyMed (National Library of Medicine), updated Oct 28, 2022

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