NDC 0409-1402

Heparin Sodium 5000 [USP'U] per 1 mL injection, solution

On the label: Hospira, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hospira, Inc.McPherson, KS, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action
Hospira, Inc.Rocky Mount, NC, United StatesTests it No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action

Product details

Generic drug
Heparin: every company that makes it
Form
injection, solution
Strength
5000 [USP'U] per 1 mL
Approval
ANDA ANDA088100
On the market since
Feb 18, 2011
Package NDCs
0409-1402-12 0409-1402-27
Official label
DailyMed (National Library of Medicine), updated Aug 25, 2026

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