NDC 31722-175

Methylphenidate Hydrochloride 20 mg tablet

On the label: Camber 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, oral
Strength
20 mg
Approval
ANDA ANDA207416
On the market since
Oct 1, 2015
Package NDCs
31722-175-01 31722-175-05
Official label
DailyMed (National Library of Medicine), updated Aug 6, 2025

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