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Dexmethylphenidate Hydrochloride Extended-Release

NDC 0781-2731 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namedexmethylphenidate hydrochloride
Labeler / ManufacturerSandoz Inc
Marketing categoryNDA AUTHORIZED GENERIC · App NDA021802
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (25 mg/1)
Marketing started20261001
Package count1

External sources

Source: openFDA. Public-domain (CC0).