Pharmacy Benefits Management

July 1, 2024

GENERIC DRUG APPROVALS – July 2024

July 2024 - GENERIC DRUG APPROVALS
Indium In-111 Pentetreotide Injection Kit 3mCi/mL
Approved: July 1, 2024 - Sun Pharmaceutical Industries, Inc.
Used for: Diagnosis and Investigation
Generic for: Octreoscan

February 14, 2024

CDC May Consider Loosening COVID Isolation Guidance

February 14, 2024 - By Robin Foster HealthDay Reporter, Medically reviewed by Carmen Pope, BPharm.
New, proposed guidance being weighed by the U.S. Centers for Disease Control and Prevention recommends that Americans

February 13, 2024

Scientists Develop Sensor That Tests Saliva for Breast Cancer

February 13, 2024 - By Dennis Thompson, HealthDay Reporter, Medically reviewed by Carmen Pope, BPharm.
Mammograms are a lifesaving misery for middle-aged women, but a new tool could make getting a breast cancer screening as easy as spitting.

February 13, 2024

Ipsen’s Onivyde Regimen, a Potential New Standard-of-Care First-Line Therapy in Metastatic Pancreatic Adenocarcinoma (mPDAC), Approved by the FDA

February 13, 2024 – Ipsen has announced that the U.S. Food and Drug Administration has approved the

February 12, 2024

Azurity Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Zenzedi® (dextroamphetamine sulfate tablets, USP) 30 mg Due to a Mislabeled PackageDuring Manufacturing

January 24, 2024 – Azurity Pharmaceuticals, Inc. is voluntarily recalling one (1) lot (F230169A) of Zenzedi^®

GENERIC DRUG APPROVALS – July 2024

CDC May Consider Loosening COVID Isolation Guidance

Scientists Develop Sensor That Tests Saliva for Breast Cancer

Ipsen’s Onivyde Regimen, a Potential New Standard-of-Care First-Line Therapy in Metastatic Pancreatic Adenocarcinoma (mPDAC), Approved by the FDA

FDA Approves Eohilia (budesonide oral suspension) for the Treatment of Eosinophilic Esophagitis

Generic Drug Approvals

Generic Drug Approvals Bromfenac

Azurity Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Zenzedi® (dextroamphetamine sulfate tablets, USP) 30 mg Due to a Mislabeled PackageDuring Manufacturing