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For pediatric patients ages 12 and over, the maintenance dose is 2.4 mg once weekly

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These actions improve glucose control in type 2 diabetes patients who have weak GLP-1 response

It is expected to be commercially available by 2026 or 2027, after the FDA approves the medication.

Red Flags When Evaluating a Peptide Vendor Suppliers whose labeling or website language implies human use, suggests therapeutic effects, or markets the compound by comparison to FDA-approved drugs were the focus of the FDA's enforcement actions in 2025 and 2026 [5][14][15][16]

The impact of tirzepatide and glucagon-like peptide-1 receptor agonists on oral contraceptive exposure