FDA NDC Directory · JSON-LD · Markdown

methylphenidate hydrochloride

NDC 0591-3873 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208861
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (30 mg/1)
Marketing started20200930
Package count1

External sources

Source: openFDA. Public-domain (CC0).