Sivextro

Active Ingredient(s): Tedizolid Phosphate
FDA Approved: * June 20, 2014
Pharm Company: * CUBIST PHARMS
Category: Skin Care

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Sivextro Overview

Tedizolid (formerly torezolid, trade name Sivextro),[1] is an oxazolidinone-class antibiotic. Tedizolid phosphate is a phosphate ester prodrug of the active compound tedizolid. It was developed by Cubist Pharmaceuticals, following acquisition of Trius Therapeutics (originator: Dong-A Pharmaceuticals), and is marketed for the treatment of acute bacterial skin and skin structure infections (also known as complicated skin and skin-structure infections (cSSSIs)).[2]...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Tedizolid

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Possible Dosages for this and Related Drugs:

Tedizolid Phosphate
  • Injection: 200mg
  • Powder: 200mg/vial
  • Tablet: 200mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Sivextro: (2 results)

Sorted by National Drug Code
  • 67919-040 Sivextro 200 mg Intravenous Powder, for Solution by Cubist Pharmaceuticals, Inc.
  • 67919-041 Sivextro 200 mg Oral Tablet, Coated by Cubist Pharmaceuticals, Inc.

Other drugs which contain Tedizolid Phosphate or a similar ingredient: (1 result)






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