NDC 73539-001

Lantidra 5000 [arb'U] per 400 mL solution

On the label: CellTrans Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
CellTrans Inc.Chicago, IL, United StatesMakes the active ingredient Not inspected on record

Product details

Generic drug
Donislecel: every company that makes it
Form
solution, intravascular
Strength
5000 [arb'U] per 400 mL
Approval
BLA BLA125734
On the market since
Jun 28, 2023
Package NDCs
73539-001-01
Official label
DailyMed (National Library of Medicine), updated Jan 13, 2026

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