Cutaneous Lupus Erythematosus

• FDA approval · 2008-02-20
  FDA Approved: HYDROXYCHLOROQUINE SULFATE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved a supplemental application for hydroxychloroquine sulfate submitted by Teva Pharmaceuticals USA, Inc. The action represents an …

• FDA approval · 2007-06-14
  FDA Approved: HYDROXYCHLOROQUINE SULFATE — Original Application (Ipca Laboratories Limited)

  FDA approved Ipca Laboratories Limited's original application for hydroxychloroquine sulfate as a generic product.