FDA
approval
· 2021-02-19
FDA Approved: FAMOTIDINE — Supplemental Application (Chartwell RX, LLC)
Summary
FDA approved a supplemental application for famotidine submitted by Chartwell RX, LLC (ANDA 075786). It authorizes changes to the approved generic product.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for FAMOTIDINE (FAMOTIDINE)