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Methylphenidate Hydrochloride Extended-Release

NDC 0406-1850 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namemethylphenidate hydrochloride
Labeler / ManufacturerSpecGx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203583
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (50 mg/1)
Marketing started20150929
Package count1

External sources

Source: openFDA. Public-domain (CC0).