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News

  American Regent announces new PDUFA action date for Injectafer® (ferric carboxymaltose injection) NDA for the treatment of iron deficiency anemia
4/8/2013
  Epinephrine Injection, USP Important Drug Administration Information
2/5/2013
  Methylergonovine Heathcare Professional Letter
12/20/2012
  American Regent Anounces an FDA Pediatric Indication Exclusivity for Venofer (Iron Sucrose Injection, USP)
10/19/2012
  American Regent announces a new FDA-Approved Pediatric Indication for Venofer® (Iron Sucrose Injection, USP)
9/26/2012
  Luitpold Pharmaceuticals, Inc. Receives Complete Response Letter for Injectafer® from the U.S. Food and Drug Administration
7/26/2012
  National Registry Study Evaluating Utility of SPRIX® (ketorolac tromethamine) Nasal Spray, a Non-Narcotic Alternative for Pain Management after Emergency Department Care, Begins
6/25/2012
  American Regent Initiates Nationwide Voluntary Recall of Cyanocobalamin Injection, USP, 1000 mcg/mL, 1 mL Vial, Lot #s 1662, 1679, 1683 Due to Cracks in the Vials
4/2/2012
  FDA Assigns PDUFA Date for Injectafer® (ferric carboxymaltose injection) NDA
12/15/2011
  Important Drug Administration Information - Ammonium Molybdate Injection, USP, 250 mcg/10 mL (25 mcg/mL) 10 mL Single Dose Vial - NDC#: 0517-6610-25
11/1/2011
  Luitpold Pharmaceuticals, Inc. submits Injectafer® NDA to the U.S. Food and Drug Administration
10/13/2011
  American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials due to Sub-Potency
8/2/2011
  American Regent Initiates Voluntary Nationwide Recall of Calcium Gluconate Injection, USP, 10%,100 mL Pharmacy Bulk Package Due to Particulates
7/18/2011
  American Regent Initiates Nationwide Voluntary Recall of Methyldopate HCL Injection, USP
6/6/2011
  American Regent Initiates Nationwide Voluntary Recall of Sterile Water for Injection, USP
5/19/2011
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