Cefdinir Powder, For Suspension
Product Images NDC 68180-723

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Cefdinir (NDC 68180-723). 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.

FDA Label Image

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Chemical structure of cefdinir, depicted as a molecular diagram showing its characteristic beta-lactam ring and other chemical features consistent with the antibiotic cefdinir.*

FDA Label Image

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Label for Cefdinir for Oral Suspension USP 125 mg/5 mL powder for suspension by Lupin Pharmaceuticals, Inc. The label includes NDC 68180-722-20, reconstitution directions with 35 mL water to make 60 mL suspension, and storage instructions. It also shows manufacturing information for Lupin Limited in India and Lupin Pharmaceuticals in Baltimore, MD.*

FDA Label Image

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Cefdinir for Oral Suspension USP 250 mg/5 mL powder for suspension label by Lupin Pharmaceuticals, Inc. The 60 mL bottle label includes dosing and reconstitution instructions, a barcode, and storage information. It specifies the powder must be reconstituted with 35 mL water and shaken before use. Manufacturer details from Lupin Limited, India, are also present.*

FDA Label Image

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Label for Cefdinir for Oral Suspension USP 125 mg/5 mL powder for suspension, 60 mL bottle when reconstituted. Manufactured for Lupin Pharmaceuticals, Inc. and Lupin Limited India. Label includes dosage directions, reconstitution instructions with 38 mL water, storage conditions, and a barcode.*

FDA Label Image

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Label for Cefdinir for Oral Suspension USP 250 mg/5 mL powder for suspension, with 60 mL bottle size when reconstituted. Manufactured by Lupin Pharmaceuticals, Inc. The label includes dosage and reconstitution directions, NDC 68180-723-04, and storage instructions. The label also shows manufacturing details and a barcode.*

* 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.