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Follow-up frequency varies according to local service protocols, with more frequent reviews during dose titration, then periodic review (typically every 3-6 months) once established on treatment

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503A Compounding Pharmacies Limitations on Compounding “Copies” of Commercial Drugs The SAFE Drugs Act proposes to amend Section 503A of the FDCA to (i) codify the definition of “essentially a copy of a commercially available drug product” and (ii) prevent compounding pharmacies from compounding more than 20 units per month of any drug that is “essentially a copy” of a commercially available product unless tailored to an individual patient