NDC 43386-575

Methylphenidate Hydrochloride 20 mg tablet

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, oral
Strength
20 mg
Approval
ANDA ANDA207884
On the market since
Nov 13, 2015
Package NDCs
43386-575-01 43386-575-03 43386-575-05
Official label
DailyMed (National Library of Medicine), updated Mar 21, 2024

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