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News
06/25/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class III recall for Focalin XR (dexmethylphenidate HCl) due to incorrect labeling, affecting 7803 bottles.
The US Food and Drug Administration (FDA) has issued a Class III recall for Focalin XR (dexmethylphenidate HCl) due to incorrect labeling, affecting 7803 bottles.
The US Food and Drug...
06/25/2026
Pharmacy Learning Network
News
06/25/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for chlorthalidone tablets due to the product’s failure to meet dissolution specifications, affecting 11 460 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for chlorthalidone tablets due to the product’s failure to meet dissolution specifications, affecting 11 460 bottles.
The US Food and Drug...
06/25/2026
Pharmacy Learning Network
News
06/25/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for aripiprazole tablets due to a product mix-up, affecting 6143 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for aripiprazole tablets due to a product mix-up, affecting 6143 bottles.
The US Food and Drug...
06/25/2026
Pharmacy Learning Network
PharmLaw
06/24/2026
Hannah Musick
The Pharmaceutical Care Management Association has sued Illinois to block key provisions of the state's Prescription Drug Affordability Act, setting up a legal challenge that could shape the future of pharmacy benefit manager (PBM)...
The Pharmaceutical Care Management Association has sued Illinois to block key provisions of the state's Prescription Drug Affordability Act, setting up a legal challenge that could shape the future of pharmacy benefit manager (PBM)...
The Pharmaceutical Care...
06/24/2026
Pharmacy Learning Network
News
06/17/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class III recall for primidone tablets for cross contamination with other products, affecting 27 936 bottles.
The US Food and Drug Administration (FDA) has issued a Class III recall for primidone tablets for cross contamination with other products, affecting 27 936 bottles.
The US Food and Drug...
06/17/2026
Pharmacy Learning Network
News
06/17/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for alcohol sanitizer spray due to microbial contamination, affecting 5 drums.
The US Food and Drug Administration (FDA) has issued a Class II recall for alcohol sanitizer spray due to microbial contamination, affecting 5 drums.
The US Food and Drug...
06/17/2026
Pharmacy Learning Network
News
06/17/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class I recall for doxorubicin hydrochloride liposome injection due to the presence of particulate matter, affecting 675 vials.
The US Food and Drug Administration (FDA) has issued a Class I recall for doxorubicin hydrochloride liposome injection due to the presence of particulate matter, affecting 675 vials.
The US Food and Drug...
06/17/2026
Pharmacy Learning Network
PharmLaw
06/16/2026
Grace Taylor, MS, MA
Ahold Delhaize USA agreed to pay $40 million to resolve allegations that supermarket pharmacies reported inflated usual and customary drug prices to federal health care programs.
Ahold Delhaize USA agreed to pay $40 million to resolve allegations that supermarket pharmacies reported inflated usual and customary drug prices to federal health care programs.
Ahold Delhaize USA agreed to pay...
06/16/2026
Pharmacy Learning Network
PharmLaw
06/11/2026
Hannah Musick
A federal court has granted Eli Lilly a preliminary injunction in its lawsuit alleging a $200 million rebate fraud scheme involving Trulicity, requiring defendants to provide detailed documentation for future rebate claims and signaling...
A federal court has granted Eli Lilly a preliminary injunction in its lawsuit alleging a $200 million rebate fraud scheme involving Trulicity, requiring defendants to provide detailed documentation for future rebate claims and signaling...
A federal court has granted Eli...
06/11/2026
Pharmacy Learning Network
News
06/11/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for duloxetine delayed release capsules for Current Good Manufacturing Practice (CGMP) deviations, affecting 50 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for duloxetine delayed release capsules for Current Good Manufacturing Practice (CGMP) deviations, affecting 50 bottles.
The US Food and Drug...
06/11/2026
Pharmacy Learning Network