Section I: Submission
Enter the name, phone, fax and date for the issuer, or for the agent that manages or administers its prescription drug benefits. An issuer or agent may have prepopulated its contact information on the copy posted on its website, so start from the plan's own copy when one exists. This tells you where to fax or mail the request.
Section II: Review
Check Expedited/Urgent Review Requested only when applying the standard review time frame may seriously jeopardize the patient's life, health or ability to regain maximum function. Checking the box takes the signature and date of the prescriber or the prescriber's designee, which certifies that statement. Leave the box unchecked for routine requests.
Section III: Patient Information
Enter the patient's name, phone, date of birth and sex (Male, Female, Other or Unknown), plus street address, city, state and ZIP code. If the issuer differs from the one named in Section I, give its name here. Add the member or Medicaid ID number and the group number so the issuer can match the request to the right coverage.
Section IV: Prescriber Information
Give the prescriber's name, NPI, specialty, address, phone and fax, and the office contact name and contact phone. The issuer uses these details to reach the office with questions and to return its decision, so list a fax line and contact person who can respond during the review period.
Section V: Prescription Drug Information
Enter the requested drug name, strength, route, quantity, days' supply and expected therapy duration. Mark new therapy or continuation, with the approximate start date, and for continuation confirm adherence and effectiveness. For provider-administered drugs, add the HCPCS code, NDC and dose per administration. For a compound drug, list all ingredients in Section VI instead of here.
Section VI: Prescription Compound Drug Information
Name the compound and list each ingredient with its NDC number and quantity. The instructions require quantities in units of measure such as mg or ml, so write the unit with every amount. Complete this section only when the request is for a compound; a single-ingredient drug is fully described in Section V.
Section VII: Prescription Device Information
For a prescription device, enter the requested device name, the expected duration of use and, if applicable, its HCPCS code. Issuers that require prior authorization of a prescription device must accept this form for it, so a device request does not need a separate service form such as NOFR001.
Section VIII: Patient Clinical Information
Give the diagnosis related to the request with the current ICD version and code. List drugs the patient has taken for this diagnosis with strength, frequency, dates started and stopped or approximate duration, and the response, reason for failure or allergy. Add height and weight if applicable, drug allergies, and relevant laboratory values with dates, or attach them.
Section IX: Justification
In the space or on a separate page, provide clinical information justifying initial or ongoing therapy or an increase in dosage, strength or frequency. Explain comorbid conditions and contraindications to formulary drugs, give titration regimens or oncology staging if applicable, and give the details for any step-therapy exception under Insurance Code Section 1369.0546(c). Attach medical records, progress notes or lab reports if needed.