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FDA approval · 2024-04-01

FDA Approved: METHYLPHENIDATE HYDROCHLORIDE — Supplemental Application (Neolpharma, Inc.)

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Summary

FDA approved a supplemental application for methylphenidate hydrochloride from Neolpharma, Inc. under ANDA208737, granting approval for this generic product.

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Diseases / indications

Drugs mentioned

  • METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)

Snippet

SUPPL AP for METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)