Nimodipine Capsule, Liquid Filled
Product Images NDC 23155-512

4 FDA label images from Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc. · 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 Nimodipine (NDC 23155-512). 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 nimodipine, illustrating its molecular framework with labeled functional groups, including nitro, methyl, and ester groups, consistent with the provided active ingredient data.*
FDA Label Image

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FDA Label Image

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Nimodipine Capsules 30 mg packaging label for oral use, manufactured by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label states the product is child-resistant, Rx only, and contains 30 unit-dose capsules in 3 blister cards of 10 capsules each. Storage and handling details are included, along with note on no coating area and lot/expiration to be overprinted at production.*
FDA Label Image

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Packaging label for nimodipine capsules, 30 mg, liquid filled, oral use. The label includes three panels with the product name, strength, and usage restrictions "For Institutional Use Only," noting that the contents are packaged child-resistant. Each bottle contains 100 capsules divided into 10 blister cards of 10 capsules each. The labeler is Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. Additional information mentions storage instructions, capsule protection from light, and that lot and expiration will be overprinted at production.*

* 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.