NDC 0406-1146

Methylphenidate Hydrochloride 20 mg tablet

On the label: SpecGx LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
SpecGx LLCHobart, NY, United StatesMakes it and tests it No problems foundMar 13, 2020 · 6 inspections
SpecGx LLCSt. Louis, MO, United StatesMakes the active ingredient Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections

Product details

Generic drug
Methylphenidate: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA040300
On the market since
Nov 27, 1998
Package NDCs
0406-1146-01 0406-1146-10
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2023

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