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So far Michael Silber has created 2529 blog entries.

Florida

Gov. Ron DeSantis (R) announced the appointment of Leigh Mathes, Mark Mikhael and Darrell Miller and the reappointment of Jonathan Hickman, Cristina Medina, Dorinda Segovia and Stephen “Ryan” West to the Board of Pharmacy. These appointments are subject to confirmation by the Florida Senate.

For more information, contact NACDS’ Leigh Knotts at 803-243-7207.

2026-02-06T08:59:03-05:00February 6, 2026|Florida|

Georgia

Gov. Brian P. Kemp (R) declared a statewide State of Emergency in response to Winter Storm Gianna. This is a separate executive order from the one issued on January 22 ahead of Winter Storm Fern. Governor Kemp also directed the Emergency Management and Homeland Security Agency (GEMA/HS) to activate the State Operations Center (SOC). The current State of Emergency will run through February 6.

For more information, contact NACDS’ Leigh Knotts at 803-243-7207.

2026-02-06T08:58:29-05:00February 6, 2026|Georgia|

Maine

The state received official notification from CMS of a $190 million award for Year 1 of the federal Rural Health Transformation Program. The award will support the state’s efforts to expand access to care, improve population health, strengthen the rural health workforce, advance technology and data integration and promote the long-term sustainability of rural health systems statewide. Supporting materials to Maine’s application for funding through the Rural Health Transformation Program are available, including the Summary of Maine’s RHTP Plan and the updated State of Maine RHTP Project Narrative. For more information, visit the Rural Health Transformation Program website.

For more information, contact NACDS’ Sandra Guckian at 703-774-4801.

2026-02-06T08:57:20-05:00February 6, 2026|Maine|

Minnesota

The Department of Health (MDH) announced it provided the Prescription Drug Affordability Board (PDAB) with the first list of drugs that meet the statutory criteria for potential cost review. In total, MDH reported that 1,083 prescription drug products met at least one of the statutory criteria—and many drugs met multiple criteria or the same criterion multiple times. The statutory criteria include thresholds for significant price increases (such as price increases exceeding 15% in a year) and expensive drugs (such as prices of more than $60,000 per year or course of treatment). The PDAB was established to conduct cost reviews of prescription drug products and has authority to set payment limits. The Board began its work in 2024 and is comprised of seven voting members appointed by the Governor and two nonvoting legislative members.  

To learn more about the PDAB, to attend a public meeting of the PDAB, or to submit comments to the PDAB, please visit the PDAB website. Stakeholders interested in receiving announcements on prescription drug price transparency at MDH may subscribe to Prescription Drug Price Transparency updates 

For more information, contact NACDS’ Jill McCormack at 717-592-8977.

2026-02-06T08:56:49-05:00February 6, 2026|Minnesota|

Nebraska

The state received a preliminary notice of award from CMS for approximately $218 million for the first year, which is more than what was budgeted for in the application materials. Due to the increased amount of the award, the state must revise some of the application materials that were submitted. Those revised documents must be submitted to and approved by CMS before work can begin. The state intends to release multiple Requests for Applications (RFA) as opportunities for organizations to apply for funds and assist with implementing this important work. To learn more about project initiatives, view the Project Narrative .​

For more information, contact NACDS’ Sandra Guckian at 703-774-4801.

2026-02-06T08:56:12-05:00February 6, 2026|Nebraska|

New Jersey

It is NACDS’ understanding that before departing office, former Gov. Phil Murphy (D) rescinded Executive Order 415a COVID-era measure that allowed advanced practice nurses (APNs) and physician assistants (PAs) to prescribe without a collaborative agreement with a physician. According to various online reportsthe rescission will go into effect on February 16. NACDS cautions members to be aware of this change in policy when filling prescriptions from non-physician providers.

For more information, contact NACDS’ Jill McCormack at 717-592-8977.

2026-02-06T08:55:34-05:00February 6, 2026|New Jersey|

North Dakota

Medicaid engaged Myers and Stauffer, LC, to perform a pharmacy cost of dispensing study. The survey is expected to be mailed on February 17. Please review the Cost of Dispensing Survey Draft. A stakeholder meeting was held on January 27; the presentation materials and recording are available online at 
North Dakota Department of Health and Human Services Provider Portal | Myers & Stauffer. Please contact the Myers and Stauffer help desk by email disp_survey@mslc.com or phone 1-800-591-1183. Please note that the help desk phone number has been updated following the January 21 announcement of the stakeholder meeting. 

 

Also in North Dakota, the state's lawmakers approved the Rural Health Transformation Program funding. The state is currently waiting for CMS to approve the grant application. Once approved, the Department of Health and Human Services will post grant opportunities on the Rural Health Transformation Funding Opportunities website. Please sign up for updates on the Rural Health Transformation Program.   

 

Finally in North Dakota, Medicaid provided the following coverage and manufacturer updates. 

Coverage Update: Formoterol 

Effective January 15: Formoterol was no longer a preferred long-acting beta agonist (LABA) and requires PA [prior authorization]. 

  • Arformoterol and Serevent Diskus remain preferred LABAs and do not require PA. 
  • Please work with prescribers to transition members to therapeutically appropriate covered alternatives. 

 

Manufacturer Update: Pulmicort Flexhaler 

Pulmicort Flexhaler is transitioning NDCs due to a new manufacturer/distributor. New Pulmicort Flexhaler NDCs with labeler code 85612 are not covered by Medicaid.  

  • The new distributor (labeler code 85612) does not participate in the Medicaid Drug Rebate Program (MDRP). 
  • Please work with prescribers to transition members to therapeutically appropriate covered alternatives. 
  • Medicaid preferred inhaled corticosteroids that do not require PA include:  
  • Arnuity Ellipta 
  • Asmanex HFA 
  • Asmanex Twisthaler 
  • budesonide suspension 
  • fluticasone HFA for members 4 years of age and younger. 

 

Medicaid cannot pay for a drug when the manufacturer does not participate in the MDRP due to federal law, Sec.1927. [42. U.S.C. 1396r-8] (a) 

  • Manufacturers choose whether they will sign up for the MDRP. 
  • Manufacturer participation is outside of Medicaid's control. 
  • An alternative, participating manufacturer's product or different drug that is covered, must be used for Medicaid to be able to pay. 

 

Coverage Update: ICS [Inhaled Corticosteroids]/LABA [Long-Acting Beta-Agonist] Inhalers 

Effective February 9, Advair HFA and Advair Diskus will be non-preferred status and require PA.  

  • Dulera will be the only ICS/LABA inhaler that does not require PA. 
  • All other ICS/LABA inhalers remain non-preferred status and require PA. 
  • Please work with prescribers to transition members now to avoid treatment disruption. 

 

Dulera contains formoterol and can be used for single-inhaler maintenance-and-reliever therapy (SMART) as recommended in asthma guidelines. Medicaid allows up to two Dulera inhalers per 30-day supply for SMART use.

Effective immediately, claims will reject for strengths that are not indicated for the member's age.  

  • Electronic age verification occurs during adjudication at the point of sale. 
  • Please work with the prescriber to use a compendia- and guideline-supported regimen. 

 

Coverage Update: Estrogen Patches 

 

Effective immediately:  

 

  • Climara is now preferred (brand is required – bill with DAW 9) and does not require PA. 
  • Menostar is no longer preferred and requires PA. 
  • Generic weekly estradiol patch is no longer preferred and requires PA. 

 

  • Minivelle is no longer preferred and requires PA. 
  • Vivelle-Dot remains preferred (brand is required – bill with DAW 9) and does not require PA. 
  • Generic twice weekly estradiol patch remains non-preferred and requires PA. 
  • Dotti remains non-preferred and requires PA. 
  • Lyllana remains non-preferred and requires PA. 

 

 

 

Coverage Update: Triptans – Nasal Spray & Injectable 

 

Effective immediately:  

 

  • Sumatriptan nasal spray is no longer preferred and requires PA. 
  • Zolmitriptan nasal spray is now preferred and requires PA. 
  • Sumatriptan vial now requires PA. 

 

 

 

Coverage Update: Interferons 

 

Effective February 1:  

 

  • Rebif was no longer preferred and requires PA. 
  • Betaseron was no longer preferred and requires PA. 
  • Avonex remains preferred and does not require PA.

Coverage Update: Miscellaneous  

Movantik: Effective February 1:  

  • Movantik was no longer preferred and requires PA. 
  • Lubiprostone and Symproic remain preferred and do not require PA. 

Entresto: Effective immediately:  

 

  • Brand Entresto is no longer preferred and requires PA. 
  • Generic sacubitril/valsartan is preferred and does not require PA. 

Topical lidocaine: PA [Prior authorization] is required, but the PA requirement was not being applied to some NDCs during claim adjudication. The system has been updated for those NDCs, so PA is required effective immediately. 

For more information, contact NACDS’ Sandra Guckian at 703-774-4801.

2026-02-06T08:54:54-05:00February 6, 2026|North Dakota|

Oregon

Below are highlights from a recent review of the state's Rural Health Transformation Program website. Members are encouraged to review the website for additional insights into the state's plan. Also, please sign up for the newsletter to receive updates directly. For questions or additional information, please contact: RHTP@oha.oregon.gov.  

RHTP Timeline 

Anticipated medium-term activities in 2026 include:  

  • Spring 2026: Oregon begins releasing Request for Grant Application (RFGA) to support approved RHTP initiatives. 
  • Early Summer 2026: RFGA response deadlines. 
  • By Mid-2026: RFGA awardee decisions announced by OHA. 

Anticipated long-term activities in 2027 and beyond include:  

  • By September 30, 2027: Federal Fiscal Year (FFY) 2026 RHTP distributions used. 
  • October 1, 2027 – September 30, 2031: Additional RHTP distributions used in subsequent FFYs. 
  • September 30, 2031: RHTP funding ends. 

December 2, 2025, Informational Webinar: Please note Implementation/Distribution Timeline and Next Steps. 

Rural Health Transformation Program: Allowable Use of Funds: Visit the Rural Health Transformation Program website and scroll down to "Rural Health Transformation Program: Allowable Use of Funds".  

Frequently Asked Questions: Please note that these will be updated regularly. (Accessed on February 3, 2026) Visit the Rural Health Transformation Program website and scroll down to "Frequently Asked Questions:" Below are the categories of information. 

  • General 
  • Application and award 
  • Use of funds and limitations 
  • Program eligibility 
  • Program design 

Also in Oregon, the Prescription Drug Affordability Board (PDAB) posted its draft agenda for the February 18 meeting. Check the PDAB website for updates to the agenda and the meeting materials. Register in advance. 

For more information, contact NACDS’ Sandra Guckian at 703-774-4801.

2026-02-06T08:53:53-05:00February 6, 2026|Oregon|
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