NDC 43386-570

Methylphenidate Hydrochloride 2.5 mg tablet, chewable

On the label: Lupin Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Methylphenidate: every company that makes it
Form
tablet, chewable, oral
Strength
2.5 mg
Approval
ANDA ANDA204115
On the market since
Apr 6, 2015
Package NDCs
43386-570-01
Official label
DailyMed (National Library of Medicine), updated Dec 11, 2023

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