An Information Service of the Division of Medical Assistance North Carolina Medicaid Pharmacy Newsletter Number 156 March 2008 In This Issue. Additional OTCs Added to the Over-the-Counter Medications Coverage List Deleted NDCs from CMS New Pharmacy Prior Authorization Program for Second Generation Antihistamines FORM Quarterly Letter Update Program of All-Inclusive Care for the Elderly (PACE) Recipient Eligibility Program New SmartPA Pharmacy Prior Authorization Program National Provider Identifiers for End-Dated Providers National Provider Identifier and Address Information Database Tax Identification Information Changes in Drug Rebate Manufacturers
Published by EDS, fiscal agent for the North Carolina Medicaid Program
Additional OTCs Added to the Over-the-Counter Medications Coverage List
The following OTC products became available for reimbursement by NC Medicaid in conjunction with a prescription order by the physician. Drug Label Name Effective Date
00781528364 CETIRIZINE HCL 5 MG CHEW TAB
00781528464 CETIRIZINE HCL 10 MG CHEW TAB
57664054088 CETIRIZINE HCL 5 MG CHEW TAB
The list of covered OTC drug codes is available on the NC Division of Medical Assistance Web site in General Medical Policy A-2 and can be found at http://www.ncdhhs.gov/dma/mp/mpindex.htm. Deleted NDCs from CMS
The following products have been deleted from the CMS Master Data Record (MDR) file of covered outpatient drugs effective as of March 17, 2008. The products do not meet the definition of a covered outpatient drug. Drug Name Drug Name
Carbetapentane Citrate/Phenylephrine HCI /Guafinesin
New Pharmacy Prior Authorization Program for Second Generation Antihistamines – Updated Implementation Date The N.C. Medicaid Outpatient Pharmacy Program will implement a new prior authorization (PA) program for second generation antihistamines on May 5, 2008. Medications that will require prior authorization include Clarinex, Allegra, fexofenadine, Xyzal and Zyrtec (prescription versions only). All over-the-counter (OTC) versions of loratadine, Claritin, cetirizine and Zyrtec will not require prior authorization. After this date, pharmacists will begin receiving a point-of- sale message that PA is required for these medications. An additional message will indicate that override at point-of-sale is allowed for these medications. If the prescriber has indicated that the PA criteria have been met, by writing one of the following phrases on the face of the prescription in his or her own handwriting, the pharmacist will be able to override the PA edit:
• For generic fexofenadine
1. “Failed loratadine and failed cetirizine for 30 days” 2. “Allergy to loratadine and cetirizine”
• For liquid formulations other than loratadine syrup and cetirizine syrup
1. “Failed loratadine and failed cetirizine syrup for 30 days” 2. “Allergy to loratadine and cetirizine syrup”
• For all other second generation antihistamines
1. “Failed loratadine for 30 days, failed cetirizine for 30 days and failed
2. “Allergy to fexofenadine, loratadine, and cetirizine”
If the second generation antihistamine has a generic version available, “medically necessary” must also be written on the face of the prescription in the prescriber’s own handwriting in order to dispense the brand name drug. A “1” in the PA field (461-EU) or a “2” in the submission clarification field (420-DK) will override the PA edit. These overrides will be monitored by Program Integrity. Providers may also contact ACS at 866-246-8505 (telephone) or 866-246-8507 (fax) to request PA for these medications. The PA criteria and request form for the second generation antihistamines are available on the N.C. Medicaid Enhanced Pharmacy Program Web site at http://www.ncmedicaidpbm.com. If the PA is approved by ACS, the POS override codes will not be needed. FORM Quarterly Letter Update Beginning in May 2008, the FORM quarterly letters that pharmacists receive indicating their patients that participate in the FORM program will include the following new features:
• The quarterly letter will include a list of recipients deleted from the program since the
• If more than one page, the quarterly letter will be combined in one envelope instead of
These changes are in addition to the new feature added to the February 2008 FORM letters which included the addition of the dates FORM recipients are entered into the FORM program. These letters will be mailed out at the end of February, May, August and November during the year. Program of All-Inclusive Care for the Elderly (PACE) Recipient Eligibility Program The Program of All-Inclusive Care for the Elderly (PACE) is a managed care program that enables elderly individuals who are certified to need nursing facility care to live as independently as possible. The PACE provider receives monthly Medicare and/or Medicaid capitation payments for each eligible enrollee. The PACE provider assumes full financial risk for participants’ care without limits on amount, duration, or scope of services. Effective February 1, 2008, to enroll in this program, an individual must be Medicaid eligible and •
Certified by the State to require nursing facility level of care;
Able to live safely in the community at the time of enrollment; and
Reside in the service area of the PACE organization.
Services provided directly by the PACE provider include, but are not limited to: •
New SmartPA Pharmacy Prior Authorization Program On April 4, 2008, North Carolina Medicaid will be implementing SmartPA to conduct point-of- sale (POS) clinical editing and pharmacy prior authorizations. SmartPA is a clinical editing and pharmacy prior authorization program that delivers pharmaceutical cost containment, efficient pharmacy benefit administration, and continued access to quality medications. Unlike other prior authorization programs, this program uses a clinical rules system, in conjunction with drug and medical claims data, to help providers determine the appropriateness of dispensing certain medications to Medicaid patients. SmartPA streamlines the prior authorization process for all stakeholders -- physicians, pharmacists, recipients, and payers. The SmartPA tool adjudicates prior authorization requests online in real time. Prescriptions that meet a predefined set of criteria are approved in seconds. A provider whose prescription is rejected by SmartPA may be instructed to contact a call center representative for prior authorization reconsideration. National Provider Identifiers for End-Dated Providers
DMA continues to adjudicate claims for providers who have been end-dated when the claims are for dates of service prior to the provider’s end-date. To date, more than 6,000 providers who were end-dated during the past 12 months have not reported their National Provider Identifier (NPI) to DMA. After May 23, 2008, claims will be denied for end-dated providers who have not reported their NPI to DMA. To report your NPI or to verify that your NPI has been received, please access the NPI and Address Information database at http://www.ncdhhs.gov/dma/WebNPI/default.htm. If all information is correct, no action is necessary. If the NPI column is blank, your NPI has not been reported. Print the form and submit your NPI with a copy of the National Plan and Provider Enumeration System (NPPES) certification. National Provider Identifier and Address Information Database The Division of Medical Assistance (DMA) has implemented a searchable National Provider Identifier (NPI) and address database. Providers can access the database by NPI or Medicaid provider number, at http://www.ncdhhs.gov/dma/NPI.htm. Please access the database as soon as possible to verify your NPI, site address, and billing address.
• If all information is correct, no action is necessary. • To correct typographical errors: print the form, make corrections, and fax to the number
• To correct more serious (non-typographical) errors, submit a Provider Change Form
(http://www.ncdhhs.gov/dma/Forms/changeprovstatus.pdf) and include any other applicable documentation.
If your NPI is not in the database, previously submitted documentation was either not sufficient to update the database or has not been submitted at all. Providers should print the form and submit your NPI with a copy of your National Plan and Provider Enumeration System (NPPES) certification. Tax Identification Information The NC Medicaid program must have the correct tax information on file for all providers. This ensures that 1099 MISC forms are issued correctly each year and that correct tax information is provided to the IRS. Incorrect information on file with Medicaid can result in the IRS withholding 28% of a provider’s Medicaid payments. The individual responsible for maintenance of tax information must receive the information contained in this article. How to Verify Tax Information The last page of the Medicaid Remittance and Status Report (RA) indicates the tax name and number on file with NC Medicaid for the provider number listed. Review the NC Medicaid RA throughout the year to ensure that the correct tax information is on file for each provider number. If you do not have access to a Medicaid RA, call EDS Provider Services at 919-851-8888 or 1- 800-688-6696 to verify the tax information on file for each provider. How to Correct Tax Information All providers are required to complete a W-9 form for each provider for whom incorrect information is on file. Please go to the following Web site to obtain a copy of a W-9 form http://www.irs.gov/pub/irs-pdf/fw9.pdf. Correct information must be received by November 1, 2008. All providers who identify incorrect tax information must submit a completed and signed W-9 form along with a completed and signed Medicaid Provider Change form http://www.ncdhhs.gov/dma/formsprov.html to the address listed below: Division of Medical Assistance - Provider Services 2501 Mail Service Center Raleigh NC 27699-2501 Changes in Drug Rebate Manufacturers The following changes are being made in manufacturers with Drug Rebate Agreements. They are listed by manufacturer code, which are the first five digits of the NDC. Additions
The following labelers have entered into Drug Rebate Agreements and have joined the rebate program effective on the dates indicated below: Code Manufacturer Date Voluntarily Terminated Labeler
The following labelers requested voluntary termination, which was effective January 1, 2008: Checkwrite Schedule Electronic Cut-Off Schedule
Electronic claims must be transmitted and completed by 5:00 p.m. on the cut-off date to be included in the next checkwrite. Any claims transmitted after 5:00 p.m. will be processed on the second checkwrite following the transmission date. POS claims must be transmitted and completed by 12:00 midnight on the day of the electronic cut-off date to be included in the next checkwrite.
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Field, temperature, and concentration dependences of the magnetic susceptibility of bismuth–antimony alloys B. Verkin Institute for Low Temperatures Physics and Engineering, National Academy of Sciencesof Ukraine, pr. Lenina 47, 310164 Kharkov, Ukraine ͑Submitted April 9, 1999; revised August 11, 1999͒ Fiz. Nizk. Temp. 26 , 54–64 ͑January 2000͒ In the framework of the McClure model,