NDC 70688-0502

Kynamro 200 mg per 1 mL injection, solution

On the label: Kastle Therapeutics, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Genzyme CorporationLocation not on fileMakes it, tests it, packages it and labels it Not inspected on record
Ionis Pharmaceuticals Inc.Carlsbad, CA, United StatesMakes the active ingredient and tests it No problems foundJan 15, 2026 · 7 inspections
AndersonBrecon Inc.Rockford, IL, United StatesPackages it and labels it No problems foundAug 19, 2026 · 11 inspections
HVL Pharma UK LimitedHaverhill, United KingdomTests it, packages it and labels it Problems found, fixed voluntarilyNov 3, 2022 · 6 inspections
International Laboratory Services, LtdLocation not on fileSterilizes it Not inspected on record

Product details

Generic drug
Mipomersen: every company that makes it
Form
injection, solution
Strength
200 mg per 1 mL
Approval
NDA NDA203568
On the market since
May 2, 2016
Package NDCs
70688-0502-1 70688-0502-2
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2017

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