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We stated in the CY 2025 PFS proposed rule (89 FR 61965) that we understand that statutory provisions at section 1860D-14B of the Act require that CMS establish the payment amount benchmark period at the dosage form and strength level, and that allowing manufacturers to reset the payment amount benchmark period for a new NDC-9 of an existing Part D rebatable drug may not fully align with this directive

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No UK Marketing Authorisation Identified No current UK marketing authorisation for a medicinal product containing 5-amino-1-methylquinolinium was identified in the official sources reviewed for this article

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