FDA
approval
· 2014-09-26
FDA Approved: PROTONIX I.V. — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
Summary
FDA approves a supplemental application for PROTONIX I.V., authorizing the intravenous form of pantoprazole sodium.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PROTONIX I.V. (PANTOPRAZOLE SODIUM)