Pulmonary Embolism

• FDA approval · 2009-07-23
  FDA Approved: HEPARIN SODIUM AND DEXTROSE — Supplemental Application (Hospira, Inc.)

  FDA approved a supplemental application for Heparin Sodium and Dextrose (Heparin Sodium) from Hospira, Inc. The approval updates the product…

• FDA approval · 2008-10-17
  FDA Approved: DRAXIMAGE MAA — Supplemental Application (Jubilant DraxImage Inc)

  FDA approved a supplemental application for the DRAXIMAGE MAA kit to prepare Tc-99m-labeled albumin aggregates for lung perfusion imaging to…

• FDA approval · 2008-10-17
  FDA Approved: ARIXTRA — Supplemental Application (Mylan Institutional LLC)

  The FDA approved a supplemental application for ARIXTRA (fondaparinux sodium) filed by Mylan Institutional LLC. The approval updates the exi…

• FDA approval · 2008-03-28
  FDA Approved: JANTOVEN — Supplemental Application (Upsher-Smith Laboratories, LLC)

  The FDA approved a supplemental application for Jantoven (warfarin sodium) filed by Upsher-Smith Laboratories, LLC.

• FDA approval · 2007-12-14
  FDA Approved: HEPARIN SODIUM — Supplemental Application (Civica, Inc.)

  FDA approved Civica, Inc.'s supplemental application for HEPARIN SODIUM. This action approves a supplemental NDA related to the product (NDA…

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• FDA approval · 2007-07-11
  FDA Approved: WARFARIN SODIUM — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved a supplemental application for Warfarin Sodium from Teva Pharmaceuticals USA, Inc. for the generic product under the ANDA.

• FDA approval · 2007-01-12
  FDA Approved: ENOXAPARIN SODIUM — Supplemental Application (Sanofi-Aventis U.S. LLC)

  FDA approved a supplemental application for ENOXAPARIN SODIUM submitted by Sanofi-Aventis U.S. LLC.

• FDA approval · 2006-10-04
  FDA Approved: HEPARIN SODIUM — Supplemental Application (Civica, Inc.)

  The FDA approved Civica, Inc.'s supplemental application for Heparin Sodium. This action updates the product labeling as part of the NDA 017…

• FDA approval · 2006-05-05
  FDA Approved: JANTOVEN — Supplemental Application (Upsher-Smith Laboratories, LLC)

  FDA approved a supplemental application for JANTOVEN (warfarin sodium) from Upsher-Smith Laboratories, LLC.