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Loteprednol Etabonate Suspension
Product Images NDC 70748-300
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Loteprednol Etabonate (NDC 70748-300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lupin Pharmaceuticals, 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 provides information about an ophthalmic suspension containing Loteprednol Etabonate, indicated for ophthalmic use only. Each mL contains 5 mg of active ingredient. The usual dosage guidance can be found in the package insert. The product should be stored upright between 15° to 25°C (59° to 77°F) and should not be frozen. It is manufactured by Lupin Limited in India. It is recommended to shake the suspension vigorously before use.*
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This is a description of a medication labeled as Lupin® Loteprednol Etabonate Ophthalmic Suspension 0.5% in a 15 mL bottle. It contains 5 mg of Loteprednol Etabonate per mL and a preservative called Benzalkonium Chloride 0.01%. The suspension is isotonic and sterile, meant for Ophthalmic Use Only. Instructions for storage between 15° to 25°C (59° to 77°F) and a warning to not freeze the product are provided. The product should be shaken vigorously before use. The manufactured information states that it is manufactured for Lupin Pharmaceuticals, Inc., in the United States, and produced by Lupin Limited in India. Batch coding and additional details will be overprinted at the plant.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
