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As a pharmaceutical producer, what you are promoting is determined by sufferers gaining access to the medications they need. The aim of regulating imprinting is to enable identification of the capsule ingredients and drug producer by legislation enforcement officials, health care suppliers and the patient or caregiver. Furthermore, Congress should harmonize generic substitution guidelines for small molecules and biologic drugs, so that sucralfate FDA-approved biosimilars can be robotically substituted by pharmacists for branded products.

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