NDC 0115-1802

Methylphenidate Hydrochloride 20 mg tablet

On the label: Amneal Pharmaceuticals.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals of New York, LLCBrookhaven, NY, United StatesMakes it, tests it and packages it No problems foundSep 25, 2026 · 14 inspections
Veranova, L.P.West Deptford, NJ, United StatesMakes the active ingredient Problems found, fixed voluntarilyJan 23, 2026 · 8 inspections

Product details

Generic drug
Methylphenidate: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA091159
On the market since
Apr 7, 2014
Package NDCs
0115-1802-01
Official label
DailyMed (National Library of Medicine), updated Feb 19, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?