FDA
approval
· 2019-07-22
FDA Approved: IBUPROFEN — Supplemental Application (Chartwell RX, LLC)
Summary
The FDA approved a supplemental application for ibuprofen from Chartwell RX, LLC under ANDA 202413, authorizing the specified changes to this generic product.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for IBUPROFEN (IBUPROFEN)