NDC 0409-5555

Sodium Bicarbonate 42 mg per 1 mL injection, solution

On the label: Hospira, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hospira, Inc.Rocky Mount, NC, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 7, 2025 · 11 inspections, 3 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 ANDA202981
On the market since
Oct 21, 2019
Package NDCs
0409-5555-02 0409-5555-12
Official label
DailyMed (National Library of Medicine), updated Apr 6, 2026

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