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Levothyroxine Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 70710-1835
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 70710-1835). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Zydus Pharmaceuticals Usa 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.
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This text is a detailed description of Levothyroxine Sodium for Injection, a medication used for intravenous use. Each vial contains 100 mcg of levothyroxine sodium and other additives. It emphasizes sterile and preservative-free properties, and provides instructions for reconstitution before use. The medication is manufactured by Zydus Lifesciences Ltd. in India and distributed by Zydus Pharmaceuticals in the USA. Storage recommendations include protecting from light and storing between 0°C to 5°C.*
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This text is about a medication called Levothyroxine Sodium for Injection, provided in a single-dose vial containing 200 mcg of levothyroxine sodium along with mannitol and sodium hydroxide. The medication is for intravenous use, and any unused portion should be discarded. The vial is lyophilized and preservative-free. Instructions for reconstitution are provided. The product should be stored at controlled room temperature and protected from light. The medication is manufactured by Zydus Lifesciences Ltd. in Vadodara, India, and distributed by Zydus Pharmaceuticals (USA) Inc. in Pennington, NJ.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
