NDC 10702-102

Methylphenidate Hydrochloride 20 mg tablet

On the label: KVK-TECH, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Product details

Generic drug
Methylphenidate: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA206932
On the market since
May 11, 2017
Package NDCs
10702-102-01
Official label
DailyMed (National Library of Medicine), updated Jan 2, 2026

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