NDC 81565-203

Heparin Sodium 1000 [USP'U] per 1 mL injection, solution

On the label: Phlow Corp..

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
Heparin: every company that makes it
Form
injection, solution, intravenous; subcutaneous
Strength
1000 [USP'U] per 1 mL
Approval
NDA NDA017029
On the market since
Mar 7, 2022
Package NDCs
81565-203-01 81565-203-02
Official label
DailyMed (National Library of Medicine), updated May 16, 2024

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