NDC 72865-133

Methylphenidate Hydrochloride 18 mg tablet, extended release

On the label: XLCare 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
Methylphenidate: every company that makes it
Form
tablet, extended release, oral
Strength
18 mg
Approval
ANDA ANDA211009
On the market since
Feb 24, 2020
Package NDCs
72865-133-01
Official label
DailyMed (National Library of Medicine), updated Aug 17, 2021

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