Simvastatin Tablet, Film Coated
Product Images NDC 68180-479

9 FDA label images from Lupin Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Simvastatin (NDC 68180-479). 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 diagram of the active ingredient Simvastatin, showing its molecular configuration with labeled atoms and bonds.*
FDA Label Image

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Simvastatin Tablets USP 5 mg film-coated tablets label from Lupin Pharmaceuticals, Inc. The label includes storage instructions to keep at 20° to 25°C and cautions to preserve in a tight container. The package contains 1000 tablets and includes manufacturer information for Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and Lupin Limited, India. The NDC is 68180-482-03.*
FDA Label Image

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Label for Simvastatin Tablets USP 10 mg by Lupin Pharmaceuticals, Inc., showing a package quantity of 1000 tablets. The label includes storage instructions, usual adult dosage reference, barcode, and manufacturer details from Lupin Pharmaceuticals in the US and Lupin Limited in India.*
FDA Label Image

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Label for Simvastatin Tablets USP 20 mg film-coated tablets, packaged in a container of 1000 tablets. The label includes the NDC 68180-479-03 and indicates it is a prescription product from Lupin Pharmaceuticals, Inc. The label instructs storage at controlled room temperature (20° to 25°C) and notes manufacturing by Lupin Limited in Goa, India.*
FDA Label Image

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Simvastatin Tablets USP 20 mg label from Lupin Pharmaceuticals, Inc. The label states the product contains film-coated tablets, each with 20 mg simvastatin. It includes storage instructions, a barcode, and manufacturing details indicating Lupin Limited in India and Lupin Pharmaceuticals in the United States. The package size indicated is 1000 tablets.*
FDA Label Image

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Simvastatin Tablets USP 40 mg film-coated tablets packaging label. The label shows the strength as 40 mg and states that each tablet contains simvastatin USP 40 mg. It also indicates a count of 1000 tablets and includes storage instructions and manufacturer details for Lupin Pharmaceuticals, Inc. and Lupin Limited.*
FDA Label Image

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Simvastatin Tablets USP 40 mg film-coated tablets label from Lupin Pharmaceuticals, Inc. The label shows the strength as 40 mg and indicates each tablet contains simvastatin USP 40 mg. The package count is 1000 tablets. Storage instructions and manufacturing information for Lupin Pharmaceuticals, Inc. in Baltimore and Lupin Limited in India are also visible, along with an NDC barcode.*
FDA Label Image

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Label for SIMVASTATIN Tablets USP 80 mg by Lupin Pharmaceuticals, Inc. The film-coated tablet contains 80 mg of simvastatin. The label indicates prescription use (Rx only) and package size of 1000 tablets. Storage instructions specify 20° to 25°C. Manufactured by Lupin Limited, India and distributed by Lupin Pharmaceuticals, Baltimore, Maryland, USA.*
FDA Label Image

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5cc0d125 B05a 479e B6bf 2bd1719d4d3e 09
Simvastatin Tablets USP 80 mg label showing a film-coated tablet strength of 80 mg. The label includes storage instructions to keep at controlled room temperature (20° to 25°C), and it states the package contains 1000 tablets. Manufactured for Lupin Pharmaceuticals, Inc. and manufactured by Lupin Limited, India. The label also features a barcode and Lupin branding with a green vertical stripe on the left.*

* 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.