Lidocaine Topical – Lidocaine 5% Ointment Prior Authorization (with Quantity Limit) Criteria - Medicare Part D
Prior Authorization and Quantity Limit Criteria for Approval
Lidocaine 5% ointment will be approved when BOTH of the following are met:
- The requested medication will be used for ONE of the following:
- Anesthesia of accessible mucous membranes of the oropharynx
OR - Anesthetic lubricant for intubation
OR - Temporary relief of pain associated with minor burns, including sunburn, abrasions of the skin, and insect bites
OR - Another indication that is supported in CMS approved compendia (e.g., cancer pain) for the requested medication AND ONE of the following:
- The patient has tried and had an inadequate response to a conventional therapy [e.g., gabapentin, pregabalin, oral prescription NSAID (non-steroidal anti-inflammatory drug)] for the requested indication
OR - The patient has an intolerance or hypersensitivity to a conventional therapy
OR - The patient has an FDA labeled contraindication to a conventional therapy
AND
- The patient has tried and had an inadequate response to a conventional therapy [e.g., gabapentin, pregabalin, oral prescription NSAID (non-steroidal anti-inflammatory drug)] for the requested indication
- Anesthesia of accessible mucous membranes of the oropharynx
- ONE of the following:
- The requested quantity (dose) does NOT exceed the program quantity limit
OR - BOTH of the following:
- The requested quantity (dose) is greater than the program quantity limit
AND - The prescriber has provided information in support of therapy with a higher dose for the requested indication
- The requested quantity (dose) is greater than the program quantity limit
- The requested quantity (dose) does NOT exceed the program quantity limit
Length of Approval: 12 months
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