Verapamil Hydrochloride Tablet
Product Images NDC 70771-1953

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Verapamil Hydrochloride (NDC 70771-1953). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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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Label for Verapamil Hydrochloride Extended-Release Tablets, USP, 120 mg by Zydus Lifesciences Limited. The packaging indicates 100 tablets per bottle for oral use. The label includes dosage strength, manufacturer details, barcode, NDC number 70771-1953-1, and storage instructions. It is a prescription drug with child-resistant packaging.*
FDA Label Image

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The label for Verapamil Hydrochloride Extended-Release Tablets, USP, strength 180 mg, features the product name prominently with the dosage in a pink box. It indicates a package size of 100 tablets for prescription use only, distributed by Zydus Pharmaceuticals (USA) Inc. Additional text notes storage conditions and child-resistant packaging. The label includes the NDC number 70771-1954-1 and a barcode on the left.*
FDA Label Image

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Image (75856e69 15d6 4982 895a 2c9e76e8020f 03)
Label for Verapamil Hydrochloride Extended-Release Tablets, USP 240 mg oral tablets by Zydus Lifesciences Limited. The label indicates a package of 100 tablets, child-resistant packaging, and storage instructions at controlled room temperature. Distributed by Zydus Pharmaceuticals (USA) Inc.*

* 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.