NDC 57664-376

Dexmethylphenidate hydrochloride 2.5 mg tablet

On the label: Caraco Pharmaceutical Laboratories, Ltd..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ohm Laboratories Inc.New Brunswick, NJ, United StatesMakes it No problems foundOct 31, 2024 · 22 inspections

Product details

Generic drug
Dexmethylphenidate: every company that makes it
Form
tablet, oral
Strength
2.5 mg
Approval
ANDA ANDA201231
On the market since
Sep 26, 2013
Package NDCs
57664-376-08 57664-376-13 57664-376-18 57664-376-83 57664-376-88
Official label
DailyMed (National Library of Medicine), updated Jan 2, 2024

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