NDC 71394-415

Luxturna 0.05 mg kit

On the label: Spark Therapeutics, Inc..

United Kingdom: 1United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Nova Laboratories LtdWigston, United KingdomMakes it Problems found, fixed voluntarilyFeb 28, 2019 · 3 inspections
Spark Therapeutics, Inc.Philadelphia, PA, United StatesMakes the active ingredient and tests it Not inspected on record
Catalent CTS (Edinburgh) LimitedEdinburgh, United KingdomPackages it and labels it Not inspected on record

Product details

Generic drug
Voretigene Neparvovec: every company that makes it
Form
kit
Strength
0.05 mg
Approval
BLA BLA125610
On the market since
Dec 19, 2017
Package NDCs
71394-065-01 71394-415-01 71394-716-01
Official label
DailyMed (National Library of Medicine), updated May 1, 2022

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