NDC 43602-331

Dexmethylphenidate Hydrochloride 25 mg capsule, extended release

On the label: Ascent Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Dexmethylphenidate: every company that makes it
Form
capsule, extended release
Strength
25 mg
Approval
ANDA ANDA215523
On the market since
Dec 8, 2021
Package NDCs
43602-331-05 43602-331-30
Official label
DailyMed (National Library of Medicine), updated Dec 10, 2021

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