FDA
approval
· 2024-04-01
FDA Approved: METHYLPHENIDATE HYDROCHLORIDE — Supplemental Application (Neolpharma, Inc.)
Summary
FDA approved a supplemental application for methylphenidate hydrochloride from Neolpharma, Inc. under ANDA208737, granting approval for this generic product.
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)