Levothyroxine Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 70710-1834

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 70710-1834). 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.

FDA Label Image

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Chemical structure of levothyroxine sodium, shown as a molecular diagram with iodine atoms, hydroxyl, amine, and carboxylate functional groups clearly depicted.*

FDA Label Image

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Packaging label for Levothyroxine Sodium for Injection 100 mcg per vial, powder lyophilized for intravenous use. The label includes storage and reconstitution instructions, manufacturer Zydus Lifesciences Ltd., and distributor Zydus Pharmaceuticals (USA) Inc. The design features purple and white colors with a QR code and barcode.*

FDA Label Image

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Packaging label for Levothyroxine Sodium for Injection 200 mcg per vial, an intravenous lyophilized powder for solution. The label includes dosage strength, storage and reconstitution instructions, manufacturer Zydus Lifesciences Ltd., and distributor Zydus Pharmaceuticals USA Inc. It is a single-dose vial with directions to discard unused portions.*

FDA Label Image

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Packaging label for Levothyroxine Sodium for Injection, 500 mcg per vial, lyophilized powder for intravenous use. The label states preservation details, storage instructions, and reconstitution directions. Manufactured by Zydus Lifesciences Ltd. and distributed by Zydus Pharmaceuticals USA Inc. It includes barcode, QR code, and usage instructions indicating single-dose vial and disposal of unused portions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.