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Retatrutide is expected to follow a similar timeline to tirzepatide: approximately 3-4 years from Phase 3 start to FDA approval, plus several months for manufacturing scale-up
However, compounded drugs do not undergo the same rigorous FDA approval process as commercial products
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Lactic acid typically causes milder reactionsmaybe slight tingling or temporary redness that subsides quickly
The solution contains sodium phosphate buffers, sodium chloride, and other compounds that help preserve the medication's potency over time
