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Dexmethylphenidate hydrochloride

NDC 0115-1685 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079108
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (20 mg/1)
Marketing started20151221
Package count1

External sources

Source: openFDA. Public-domain (CC0).