Tymlos Injection, Solution
Product Images NDC 70539-001
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Product Visual Gallery
This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Tymlos (NDC 70539-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Radius Health, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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This is a description of a study on patient nonvertebral fracture incidence for alendronate monotherapy. The graph shows the incidence of fractures over a period of 25 months, with alendronate treatment starting at 19 months. The study compared the efficacy of alendronate to placebo and TYMLOS over a period of 25 months.*
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TYMLOS' is a medication that is given through subcutaneous injection using a pre-filled pen. It contains 3120 mcg/1.56 mL (2000 mg/m) of ahaloparatide. The medication should be kept refrigerated until the first use, after which it can be stored at room temperature for up to 30 days. Unused portions should be discarded after 30 days. Before injecting, read the instructions for use carefully.*
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TYMLOS' (abaloparatide) injection is a prescription drug for subcutaneous use and is meant for single patient use only. Each pre-filled pen contains enough doses for 30 injections. The medication needs to be kept refrigerated at 2°C - 8°C (36°F - 46°F) before the first use and after that, it can be stored for up to 30 days at a temperature range of 20°C - 25°C (68°F - 77°F). Unused portions should be discarded 30 days after opening. Before injecting, it is important to read the instructions for use. The drug is manufactured by Radius Health, Inc. in Boston, MA.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.