NDC 49884-428

Dexmethylphenidate Hydrochloride Extended-Release 15 mg capsule, extended release

On the label: ENDO USA, Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.

Product details

Generic drug
Dexmethylphenidate: every company that makes it
Form
capsule, extended release, oral
Strength
15 mg
Approval
ANDA ANDA078992
On the market since
Nov 19, 2013
Package NDCs
49884-428-01 49884-428-10
Official label
DailyMed (National Library of Medicine), updated Jan 5, 2026

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