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DEXMETHYLPHENIDATE HYDROCHLORIDE

NDC 31722-232 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namedexmethylphenidate hydrochloride
Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215523
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (20 mg/1)
Marketing started20211208
Package count1

External sources

Source: openFDA. Public-domain (CC0).