NDC 63323-083

Sodium Bicarbonate 42 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, 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
Bicarbonate Ion: every company that makes it
Form
injection, solution, intravenous
Strength
42 mg per 1 mL
Approval
ANDA ANDA206688
On the market since
Aug 25, 2025
Package NDCs
63323-083-03 63323-083-05
Official label
DailyMed (National Library of Medicine), updated Sep 23, 2025

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