NDC 70010-014

Methylphenidate Hydrochloride 30 mg capsule, extended release

On the label: Granules Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Granules Pharmaceuticals Inc.Chantilly, VA, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyApr 3, 2026 · 6 inspections

Product details

Generic drug
Methylphenidate: every company that makes it
Form
capsule, extended release, oral
Strength
30 mg
Approval
ANDA ANDA211796
On the market since
Sep 10, 2019
Package NDCs
70010-014-01
Official label
DailyMed (National Library of Medicine), updated Oct 8, 2026

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