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FDA label_change · 2021-06-25

FDA Approved: METHYLIN — Supplemental Application (SHIONOGI INC.)

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Summary

FDA announces a supplemental application outcome for METHYLIN (methylphenidate hydrochloride) from Shionogi Inc., resulting in a labeling change.

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Diseases / indications

Drugs mentioned

  • METHYLIN (Methylphenidate hydrochloride)

Snippet

SUPPL AP for METHYLIN (METHYLPHENIDATE HYDROCHLORIDE)