Alerts page 1 of 48

Title Drug Date Published Source
Apotex Corp.Recalls Single Lot of Carbamazepine Tablets 200 mg Carbamazepine 2010-Jul-30 FDA
Paddock Laboratories, Inc. Recalls Single Lot of LiothyronineTablets Liothyronine 2010-Jul-30 FDA
McNeil Healthcare Recalls Additional Lot of Motrin IB Ibuprofen 2010-Jul-30 FDA
Vintage Pharmaceuticals LLC Recalls Single Lot of Ibudone, 5 mg/200 mg tablets Vicoprofen 2010-Jul-30 FDA
The FDA Announces Ongoing Safety Review of Evamist and Reports of Unintended Exposure of Children and Pets Estrofem 2010-Jul-29 FDA
FDA Warns about Risk of Developing Rare Type of Pneumonia During Treatment With Cubicin Daptomycin 2010-Jul-29 FDA
Bausch + Lomb Recalls PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 Soft Gel Ascorbic Acid / Copper / Retinol / Tocopherol / ZI 2010-Jul-28 Manufacturer
FDA Publishes Question and Answers about Approval of Generic Version of Lovenox (Enoxaparin Sodium Injection) Lovenox 2010-Jul-23 FDA
Glumetza: Depomed Inc. Recalls Several Lots Metformin 2010-Jul-21 FDA
Two Companies Recall Their Isosorbide Mononitrate Product Isosorbide 2010-Jul-21 FDA
Sertraline 100 mg Tablets: Single Lot Recalled Sertraline 2010-Jul-21 FDA
Zolpidem: Two Lots Recalled Because of Oversized Tablets Zolpidem 2010-Jul-21 FDA
Little Tummy's Stimulant Laxative Drops: Manufacturer Recalls Four Lots Senna Alexandrina 2010-Jul-21 FDA
Ortho-McNeil Pharmaceutical, Inc. Recalls Select Lots of Ultram ER (tramadol HCl) Extended-Release Tablets, 100 mg Tramadol 2010-Jul-21 FDA
Itch Relief Eye Drops Recalled from Popular Store Brands (Target, Walgreens, CVS, Kroger, H-E-B and Others) Ketotifen 2010-Jul-21 FDA
Amoxicillin for Oral Suspension: Recall by Teva Pharmaceuticals Trimox 2010-Jul-20 FDA
Select Lots of Nifediac CC Extended Release 60 mg Tablets Recalled By Biovail Pharmaceuticals Nifedipine 2010-Jul-20 FDA
Paroxetine 40 mg Tablets: Single Lot Recalled by Aurobindo Pharma Paroxetine 2010-Jul-20 FDA
Tretinoin Cream: Three lots recalled by Ortho Pharmaceutical Tretinoin 2010-Jul-20 FDA
Recall of Two Lots of Sulfacetamide Sodium Topical Suspension Sulfacetamide 2010-Jul-20 FDA
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