Category: Pharmacy News

  • Pharmacy News: September 11, 2026

    Four items today, led by a California sentencing that every pharmacy owner should read. Also on the list: a new federal 340B reporting system that opens October 1, another manufacturer narrowing contract pharmacy access, and a hospital taking HRSA to court over how 340B registration works. The Federal Register also carried four DEA decisions against individual prescribers, none involving a pharmacy.

    Thirty years in a $270 million Medi-Cal scheme that ran through a pharmacy

    The Justice Department announced on September 9 that Paul Richard Randall was sentenced to 30 years in federal prison and ordered to pay $178,746,556 in restitution. Prosecutors said he caused roughly $269 million in claims to be submitted to Medi-Cal over eleven months through a pharmacy called Monte Vista, and that Medi-Cal paid about $178.7 million of it. Charged with him were the pharmacist who owned the pharmacy and a nurse practitioner who, according to the government, signed pre-filled prescriptions for patients she never met. The opening the scheme used is the part worth understanding. Medi-Cal had temporarily suspended its prior authorization requirement while it moved to a new prescription payment system, and the claims went in for high-reimbursing non-contracted generics during that window, including about $13,424 for a single meloxicam prescription. The case was built on kickbacks and medical necessity, not on billing arithmetic alone. If your pharmacy is being handed prescriptions by a marketing company, this is what that can become. Read more at the U.S. Department of Justice →

    CMS opens its first Medicare 340B data repository on October 1

    CMS is set to begin accepting Medicare Part D claims data from 340B covered entities next month through a new repository, the first of its kind. Participation is voluntary at launch. That word deserves attention, because voluntary reporting systems have a way of becoming the benchmark everyone is later measured against, and the entities that submit early tend to shape what the data looks like. If you participate in 340B, this is a decision worth making deliberately in the next few weeks instead of by default. Read the program details closely before deciding what to submit. Read more at 340B Report →

    Takeda adds a blood cancer drug to its contract pharmacy restrictions

    Takeda has added a blood cancer treatment to the list of drugs it restricts through contract pharmacy arrangements. Each addition of this kind narrows where a covered entity can have a 340B prescription filled, and the margin on that drug is what is at stake for the entity and for the specialty pharmacy dispensing under contract. Manufacturer policies differ from one another in their terms and in their exceptions, so the policy itself has to be read before anyone concludes what is still permitted. If this drug moves through your pharmacy under a 340B contract, check the policy now instead of finding out at the claim. Read more at 340B Report →

    A Michigan hospital sues HRSA over the 340B registration process

    A Michigan teaching hospital has filed suit against HRSA in federal court in Washington, D.C., arguing that the agency’s 340B registration process is unlawful. Eligibility and registration disputes usually stay inside the agency, so a court challenge aimed at the mechanism itself is worth following. What the complaint actually claims, and how far it reaches, cannot be characterized before the filing is read. For covered entities, the case is one to watch instead of act on for now. Read more at 340B Report →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 10, 2026

    Two items today. A nationwide recall of three lots of injectable epinephrine that every pharmacy and infusion site should check against its own stock, and a look at what happens when a drug clears FDA before insurers are ready to pay for it.

    American Regent recalls three lots of epinephrine injection over cracked vials and particulate matter

    American Regent announced a voluntary nationwide recall on September 3 covering three lots of Epinephrine Injection, USP, 30 mg/30 mL (1 mg/mL) multi-dose vials, NDC 0517-3030-01. The affected lots are 25128L1C0, 25280L1C0 and 26108L1C0. Customer complaints described leaking and cracked vials, and the company investigation found particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass. The stated risk is serious. Particulate injected intravenously can block and clot blood vessels, and a cracked vial means sterility can no longer be assured. No adverse events had been reported at the time of the announcement. Distributors, retailers and healthcare facilities are told to stop using the product and return it to the place of purchase or discard it. This is worth a same-day check of physical stock, and of emergency kits in particular, because epinephrine usually sits in a crash box instead of on an active dispensing shelf, and stock nobody has touched in months is exactly the stock that gets missed. Read more at FDA →

    A newly approved cancer drug shows the gap between FDA approval and insurance coverage

    STAT reports on patients with pancreatic cancer caught between the approval of a new drug and the point at which insurers were ready to cover it. The drug nearly doubled median survival in its key trial. The expanded access programs that had been supplying it closed as soon as FDA approved, and coverage was not yet in place, so some patients waited weeks with nothing to bridge them. The reported cost is close to $40,000 a month, and one family paid more than $9,000 for a seven day supply while an approval worked its way through. The pattern is not unique to this drug. It repeats on most specialty launches, and the pharmacy or infusion provider is usually the one standing in front of the patient when it happens. Anyone building a specialty or infusion service should settle in advance how a launch-window gap gets handled, including who talks to the patient about cost and what the site is willing to supply at risk. Working that out for the first time with a patient waiting is the worst version of it. Read more at STAT →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 9, 2026

    Four items today. A new FDA compounding guidance that took effect on publication and reaches state-licensed pharmacies, two developments in 340B, and a federal audit of how California handles Medicaid overpayment recovery.

    FDA issues temporary compounding policies for neonatal starter parenteral nutrition

    FDA has published guidance describing its regulatory and enforcement priorities for compounding certain starter parenteral nutrition drug products for neonates. Two things stand out. The guidance was published for immediate implementation rather than going out for comment first, which usually points to a supply problem sitting behind it. And it is not limited to registered outsourcing facilities. It also covers state-licensed pharmacies and federal facilities that are not registered with FDA as outsourcing facilities. If your pharmacy compounds neonatal starter parenteral nutrition, the conditions set out in the guidance are what you will be measured against now. Those conditions are the substance of the document, so read them before assuming you are covered by the policy. Read more at the Federal Register →

    Johnson & Johnson expands 340B data requirements and extends contract pharmacy restrictions to grantees

    Johnson & Johnson has announced it will expand its 340B claims data requirements to cover drugs a covered entity dispenses in house, not only those going through contract pharmacies. It is also extending its contract pharmacy restrictions to grantees. Both halves matter. Manufacturers and covered entities have been fighting over contract pharmacy arrangements for years, and pulling grantees into the restrictions widens that fight to organizations that had largely stayed out of it. The in-house data requirement is a different kind of change, because it reaches dispensing a covered entity handles itself. Grantees in particular should expect to hear about this directly rather than read about it later. Read more at 340B Report →

    A congressional report tracks what states are doing on 340B

    A new congressional report on state efforts to lower prescription drug prices gives attention to the growing number of states that have acted on 340B. Most of that state activity has taken the form of contract pharmacy protection laws, passed while the federal litigation continues. The report is useful as a map of where the states stand and which way they are moving. It is a survey rather than a legal analysis, and it is worth reading as one. Read more at 340B Report →

    OIG says California did not return the full federal share of Medicaid overpayments

    The HHS Office of Inspector General has released an audit examining whether California reported and returned the correct federal share of Medicaid overpayments identified by its Medicaid Fraud Control Unit during federal fiscal year 2023. OIG concluded the state fell short across the 26 cases it reviewed, and put the federal share that should have been reported and returned at just over $99 million. This is a finding about the state’s reporting, not about any individual provider. It is worth noting anyway, because of what tends to follow. When a state is told it left that much federal money unrecovered, pressure to pursue recovery on the provider side generally increases, and pharmacies sit in the Fraud Control Unit’s case mix alongside everyone else. Read more at the HHS Office of Inspector General →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 8, 2026

    A quiet stretch over the holiday weekend. Two items today. A federal appeals court has weighed in on the Anti-Kickback Statute and the way HHS handles advisory opinion requests, and the DEA published a registration order worth a look if you hold a registration of your own.

    A federal appeals court weighs in on the Anti-Kickback Statute and HHS advisory opinions

    The D.C. Circuit has decided Vertex Pharmaceuticals v. HHS. The reading from Frier Levitt is that the court left the Anti-Kickback Statute’s reach broad while placing real limits on how HHS evaluates and processes advisory opinion requests. If that holds, a company weighing a patient support or copay assistance program has a somewhat more predictable path to a favorable opinion, and no less exposure under the statute itself. This is an appellate opinion, so anyone planning to rely on it should read the decision rather than a summary of it, including this one. Read more at Frier Levitt →

    DEA publishes a decision and order against a physician registrant

    The Drug Enforcement Administration published its decision and order in the matter of Stephen Bossenberry, M.D., in today’s Federal Register. An individual practitioner case rarely changes how a pharmacy operates day to day. These orders are still where the agency sets out its current thinking on registration sanctions, which makes them worth following for anyone who holds a DEA registration. Read more at the Federal Register →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 4, 2026

    One to watch today. Oversight of the 340B program is reportedly moving from HRSA to CMS this month, though nothing is official yet. Below that, what covered entities can do about manufacturer data demands, and a Medicare audit finding worth knowing about.

    340B oversight may be moving from HRSA to CMS

    340B Report says the administration is expected to shift oversight of the 340B program out of HRSA and into CMS this month. It is attributed to an unnamed source and nothing has been announced, so treat it as a heads-up rather than a done deal. If it holds, it changes who writes the rules and who enforces them for covered entities and contract pharmacy arrangements alike. Read more at 340B Report →

    What covered entities can do about manufacturer 340B data demands

    Eli Lilly has already suspended 340B pricing for hospitals that did not meet its claims-data policy, and Tampa General Hospital sued over the price increases that followed. This piece is about what a covered entity can do now rather than waiting to see how the litigation lands. Worth reading if you are sitting on a manufacturer data demand and hoping it goes quiet. Read more at Frier Levitt →

    Medicare Part D paid $588 million for drugs that had gone over the counter

    A federal audit found Medicare Part D sponsors paid roughly $588 million from 2021 through 2023 for medications that had already transitioned from prescription to over-the-counter status. The HHS Office of Inspector General pointed to outdated FDA information and the lack of a clear process on the CMS side. Numbers like that tend to become audit priorities later. Read more at Pharmacy Podcast Network →

    Why the letter of intent matters more than people think

    An attorney’s view from both sides of a pharmacy deal, focused on the letter of intent and what actually protects a buyer or a seller once things get complicated. Useful background if you are thinking about buying or selling a pharmacy. Read more at Boesen and Snow Law →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 3, 2026

    A busier day than usual. California confirmed its new licensing rule for nonresident pharmacies, and a federal appeals court revived a whistleblower tool used against health care fraud. Below that, a PBM lawsuit and the latest on 340B.

    Nonresident pharmacies now need a California-licensed pharmacist-in-charge

    The Board of Pharmacy’s September update confirms it: since July 1, a nonresident pharmacy can’t ship prescriptions to California patients unless its pharmacist-in-charge holds a California license. The Board says it won’t move to shut down good-faith compliance efforts during the transition, but that’s a grace period, not a pass. Read more at California State Board of Pharmacy →

    Appeals court revives a whistleblower tool used against health care fraud

    The Eleventh Circuit reversed a district court ruling that had declared False Claims Act whistleblower suits unconstitutional. That ruling was the argument PBM and pharmacy defendants were watching closely as a way to head off fraud claims before they started. This closes that door, at least in that circuit. Read more at Frier Levitt →

    Florida’s attorney general accuses two PBMs of price fixing

    Florida sued Express Scripts and Prime Therapeutics, alleging their 2019 partnership was used to push down pharmacy reimbursement rates. Prime disputes the claim. Another sign of how closely PBM steering and reimbursement practices are drawing regulator attention. Read more at Fierce Healthcare →

    Massachusetts advances a broad PBM reform bill

    A legislative committee moved Massachusetts House Bill 4493 forward, a package aimed at PBM practices that squeeze independent and community pharmacies. It isn’t California law, but it’s the kind of bill language other states tend to borrow. Read more at Frier Levitt →

    States keep winning 340B lawsuits against drug manufacturers

    A Colorado federal judge dismissed a drug industry trade group’s challenge to that state’s 340B law, and similar fights are playing out in South Dakota, North Dakota, Maryland and West Virginia. So far, the pattern favors the states. Read more at 340B Report →

    AbbVie and Organon expand their 340B exemption lists

    Both manufacturers added new states to the list exempt from their 340B contract-pharmacy restrictions, and Amgen published a new FAQ on encounter data requirements. Worth checking if your 340B billing runs through a contract pharmacy relationship. Read more at 340B Report →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 2, 2026

    Quiet day for California Board of Pharmacy activity. One item worth a look, on how a PBM audit changes once the plan sends back a full discrepancy list instead of one number to dispute.

    When a PBM audit turns into a discrepancy list, the fight changes

    A discrepancy list breaks an audit finding into individual line items instead of a single number, and that changes how a pharmacy should respond. If your pharmacy is in the middle of a PBM audit, this is worth reading before your next response goes out. Read more at Boesen & Snow Law →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: September 1, 2026

    Posted September 1, 2026

    Quiet day for California Board of Pharmacy activity. The bigger story right now is 340B, where drug manufacturers pushed back against the program on three separate fronts this week, and mostly lost.

    Manufacturers can’t switch to a rebate model without HRSA’s sign-off

    The D.C. Circuit Court of Appeals sided with the federal government in a long-running dispute over how 340B discounts get delivered. Manufacturers that wanted to move from upfront discounts to a rebate model needed HRSA approval first, and didn’t have it. Read more at Frier Levitt →

    HRSA is asking 340B providers about their contract pharmacy agreements

    Sanofi has requested that certain 340B contract pharmacy agreements be disclosed, and HRSA has reached out to the providers involved. If your pharmacy holds a 340B contract pharmacy relationship, this is worth watching for what HRSA does next. Read more at 340B Report →

    A federal judge dismissed AstraZeneca’s challenge to Colorado’s 340B law

    It isn’t California law, but it’s the same fight (manufacturers trying to limit where 340B drugs can be dispensed) playing out state by state, and it’s another loss for the manufacturer side. Read more at 340B Report →

    CMS is being pushed to drop a proposed cut to 340B payments

    Hospital groups want CMS to abandon a proposed reduction to 340B payments under the outpatient payment rule, while two industry groups are backing the cut. The comment period is still open. Read more at 340B Report →

    A federal 340B reform bill is drawing mixed reactions

    Senator Bill Cassidy’s draft 340B reform legislation is getting pushback from providers over some of its proposed changes. Early stage, but a bill worth watching if you’re tracking federal reform. Read more at 340B Report →

    Why isn’t a PBM’s own biosimilar showing up on its own formulary?

    A recent analysis found that PBM-affiliated private-label biosimilars often aren’t covered on their own corporate siblings’ Medicare Part D formularies, even where you’d expect a built-in advantage. Useful context if you’ve ever wondered why. Read more at Drug Channels →


    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299

  • Pharmacy News: August 28, 2026

    Three items from the end of August. The one that matters most is a $50 million settlement that shows where controlled substance enforcement is pointed, and it points at the pharmacy that filled the prescription and not only at the prescriber who wrote it.

    Walmart pays $50 million over unlawful controlled substance prescriptions

    The Department of Justice announced that Walmart agreed to pay $50 million to resolve allegations that its pharmacies filled thousands of invalid prescriptions for opioids and other controlled substances. The principle underneath the case is corresponding responsibility, which places a duty on the pharmacist who fills a prescription and not only on the prescriber who wrote it. That duty is the exposure retail and independent pharmacies most often underestimate, because it does not require proof that anyone at the pharmacy knew a prescription was fraudulent. It asks instead what the pharmacy should have caught. The settlement terms are worth reading for the compliance obligations attached to them, since obligations negotiated in a case this size tend to become the practical benchmark that regulators and DEA measure smaller pharmacies against later. Read more at the Department of Justice →

    A fifth hospital sues CVS over 340B reimbursement practices

    A fifth hospital has sued CVS over its handling of 340B savings. At five suits this stops being an outlier and starts being a pattern. The claims go to whether savings meant for covered entities were captured elsewhere in the chain, which is a question that reaches well past the parties in any one case. Covered entities, and pharmacies operating under contract pharmacy arrangements, have reason to follow how these develop, because the outcomes will shape what a defensible 340B arrangement is understood to look like. Read more at Frier Levitt →

    California is using AI to support Medi-Cal reenrollment

    Hooper Lundy has a short piece on California turning to artificial intelligence to support Medi-Cal reenrollment. Nothing here asks a pharmacy to do anything today. It is worth knowing anyway, because reenrollment mechanics decide who stays covered, and coverage churn arrives at the pharmacy counter as rejected claims and as patients facing costs they did not expect. The direction the state is moving on this is worth watching. Read more at Hooper Lundy & Bookman →

    This update is general information about developments in pharmacy law and regulation. It is not legal advice, it does not create an attorney-client relationship, and it should not be relied on as a substitute for advice about your own situation. Prior results do not guarantee a similar outcome. If you have a specific question about your pharmacy, call or write and we will talk about it properly.

    Law Office of Bhavesh Desai | Bhavesh Desai, Pharm.D., Esq.
    18085 Watson Way, Yorba Linda, CA 92886 | (909) 618-7299