Felodipine Tablet, Extended Release
Product Images NDC 23155-049

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Felodipine (NDC 23155-049). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet 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 felodipine, the active ingredient in FELODIPINE extended-release tablets by Heritage Pharmaceuticals Inc. The diagram shows the molecular arrangement of felodipine with functional groups and atomic bonds clearly depicted.*

FDA Label Image

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FDA Label Image

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Label for FELODIPINE EXTENDED-RELEASE Tablets, USP 2.5 mg oral tablets. This prescription drug label indicates a package count of 100 tablets. It is manufactured by Daman Private Limited in India and distributed by Avet Pharmaceuticals Inc. The label includes storage instructions and a barcode on the right side. The brand logo 'Avet Pharma' is displayed at the bottom left.*

FDA Label Image

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FELODIPINE EXTENDED-RELEASE 5 mg oral tablets, USP, packaged as 100 tablets per bottle. The film-coated extended-release tablets are labeled for prescription use only and manufactured by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label includes storage instructions and a barcode.*

FDA Label Image

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Label for FELODIPINE Extended-Release Tablets, USP 10 mg by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label indicates 100 tablets per bottle and specifies 'Rx only.' It includes storage instructions, dosage details, and manufacturer information. The Avet Pharma logo is visible in teal on the bottom 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.