Cefixime Powder, For Suspension
Product Images NDC 68180-405

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Cefixime (NDC 68180-405). 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 the active ingredient cefixime, showing its molecular arrangement including the beta-lactam ring, amino group, and carboxylic acid functional groups, as well as the hydrate form with three water molecules.*

FDA Label Image

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Cefixime for Oral Suspension USP 100 mg/5 mL oral suspension label from Lupin Pharmaceuticals, Inc. The 50 mL bottle label includes reconstitution instructions, storage conditions, and usage directions. It indicates the product contains 100 mg of cefixime per 5 mL when reconstituted and cautions to shake well before use. The label also features a barcode and manufacturer details for Lupin Limited, India.*

FDA Label Image

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Label for Cefixime Oral Suspension USP 200 mg/5 mL by Lupin Pharmaceuticals, Inc. The 50 mL bottle label states the powder contains 2 g cefixime trihydrate prior to reconstitution, and the suspension must be mixed with 34 mL of water. It includes storage instructions before and after reconstitution, dosing directions, and pharmacist dispensing notes.*

FDA Label Image

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Label for Cefixime for Oral Suspension USP 200 mg/5 mL, a powder for reconstitution into a 75 mL oral suspension. The label includes instructions for reconstitution with 51 mL water, storage conditions, and dispensing directions. Manufactured by Lupin Pharmaceuticals, Inc. and Lupin Limited. The label is primarily green and white with red dosage highlight.*

FDA Label Image

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Label for Cefixime Capsules 400 mg manufactured by Lupin Pharmaceuticals, Inc., showing a count of 50 capsules. The label includes storage instructions, manufacturer details for Lupin Pharmaceuticals, Inc. and Lupin Limited, and cautions about household dispensing and container requirements. The NDC is 68180-416-08.*

FDA Label Image

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Label for Cefixime Capsule 400 mg, manufactured for Lupin Pharmaceuticals, Inc. The label includes the NDC number, a barcode, and spaces for lot number and expiration date. It is marked for prescription use only.*

FDA Label Image

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Packaging label for Cefixime Capsules 400 mg by Lupin Pharmaceuticals, Inc. The label specifies each capsule contains 400 mg of cefixime as the trihydrate. The package includes 10 capsules and indicates storage instructions and manufacturing details for Lupin Limited, India.*

FDA Label Image

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The image shows a label for Cefixime Capsules 400 mg manufactured by Lupin Pharmaceuticals, Inc. The label indicates a package size of 50 capsules and includes storage instructions to keep the capsules at 20 to 25°C. It features the NDC 68180-423-08 and states the product is Rx only. The label also mentions the capsules contain 400 mg of cefixime as the trihydrate and provides manufacturing details for Lupin Pharmaceuticals in Baltimore, Maryland, and Lupin Limited in India.*

FDA Label Image

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Label of Cefixime Capsule 400 mg showing the product name, strength, NDC 68180-423-11, and manufacturer Lupin Pharmaceuticals, Inc. The label includes a barcode, lot number placeholder, and expiration date placeholder.*

FDA Label Image

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Packaging label for Cefixime Capsules 400 mg by Lupin Pharmaceuticals, Inc. The label includes product name, strength, and capsule count (10 capsules). It states each capsule contains 400 mg of cefixime as the trihydrate. Dosage, storage conditions, manufacturer, and barcode are also visible on the label.*

* 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.