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Realizing this potential requires commitment to rigorous clinical research, careful attention to safety, and development of appropriate regulatory pathways that balance innovation with patient protection

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Primary Identification NDC Product Code: 73212-088 Proprietary Name: Cagrilintide Non-Proprietary Name: [1] Cagrilintide Substance Name: [2] Cagrilintide NDC Directory Status: Bulk Ingredient Product Type: [3] UNFINISHED PRODUCT INCLUDED in the NDC Directory Code Navigator: Clinical Specifications Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use