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Gastroenterology 125 (1), 136147 (2003)

The type of medication also mattered

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We also proposed, and are now finalizing, a policy that if more recent data were to subsequently become available (for example, a more recent estimate of the PPI for Pharmaceuticals for Human Use, Prescription), we would use such data, if appropriate, to determine the CY 2026 diagnostic radiopharmaceutical packaging threshold in the final rule

The TGA confirms that unapproved peptide products that are not clearly labelled, that are identified only by codes, or that do not clearly state active ingredients and dosage, cannot be assessed for lawful importation under the Scheme