NDC 13107-380

Methylphenidate Hydrochloride 5 mg tablet

On the label: Aurolife Pharma LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action
Janssen Pharmaceuticals, Inc.Athens, GA, United StatesMakes the active ingredient Problems found, fixed voluntarilyJan 24, 2025 · 5 inspections

Product details

Generic drug
Methylphenidate: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA209276
On the market since
Apr 11, 2017
Package NDCs
13107-380-01
Official label
DailyMed (National Library of Medicine), updated Oct 14, 2026

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