FDA NDC Directory · JSON-LD · Markdown

Dexmethylphenidate Hydrochloride

NDC 67877-656 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212631
Dosage form / routeTABLET · ORAL
Active ingredientsDEXMETHYLPHENIDATE HYDROCHLORIDE (5 mg/1)
Marketing started20190721
Package count3

External sources

Source: openFDA. Public-domain (CC0).