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Teva Analysts Say Migraine Drug Approval Gives Needed Relief - Bloomberg
FDA Warning Letters: May 2023 Edition
Teva Pharmaceuticals on X: "Today, the FDA approved an interchangeable #biosimilar that may provide broader access to needed medicines for patients with autoimmune diseases. Along with our partner @alvotechpr, we are proud
Teva China API plant smacked by FDA warning letter, adding to drugmaker's burdens | Fierce Pharma
The Latest Breaking News from Teva Pharmaceutical Industries Ltd – inkl news
Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride Injection USP 5 mg/5 mL Due to the Presence of Particulate Matter | FDA
Teva Set For Immediate US Launch Of Austedo In Tardive Dyskinesia :: Scrip
Teva Pharmaceuticals Receive Warning Letter from FDA – Parker Waichman LLP
Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA) | FDA
Teva Pharmaceutical | $TEVA Stock | Shares Rally After Winning FDA Approval for Migraine Therapy - Warrior Trading News
FDA warning letter says Teva China plant has more work to do on API issues | Fierce Pharma
Teva Announces FDA Approval of AUSTEDO® XR (deutetrabenazine) Extended-Release Tablets
UPDATED: Teva's struggling sterile plant hit with FDA warning letter | Fierce Pharma
ARS Pharma Shares Fall as FDA Declines to Approve Epinephrine Nasal Spray Neffy - WSJ
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules | DAIC
Alvotech & Teva Bag FDA Approval for Humira Biosimilar, Simlandi | NAVLIN DAILY
Teva halts output at U.S. drug plant after FDA flags concerns | Reuters
Teva recalls one lot of leukemia med after finding particulates in vial | Fierce Pharma
Teva Pharmaceuticals USA, Inc., Issues Voluntary Nationwide Recall of Specific Lots of Fentanyl Buccal Tablets CII Because of Labeling Error | ONS Voice
Generic Approvals Reshaping the SP Market | Anton Rx Report
Teva's troubled Godollo plant earns firm US FDA warning letter
FDA Issues Warning About Fake Adderall | Fox 8 Cleveland WJW
Warfarin Sodium by Teva Pharmaceuticals USA, Inc. WARFARIN SODIUM tablet
FDA warns fake Adderall ADD medication being sold online
FDA warns eye drops may cause infection. Here's a list of 27 products to which the alert applies. - CBS News
Teva Receives FDA Warning Letter on China API Plant