Trimethobenzamide Hydrochloride Capsule
Product Images NDC 43386-660

4 FDA label images from Lupin 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 Trimethobenzamide Hydrochloride (NDC 43386-660). 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 Trimethobenzamide Hydrochloride showing its molecular configuration including methoxy, amide, and dimethylaminoethoxy functional groups.*
FDA Label Image

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Label for Trimethobenzamide Hydrochloride Capsules USP, 300 mg, oral capsules, manufactured by Lupin Pharmaceuticals, Inc. The label includes dosage instructions, warning to dispense in a tight, well-closed container, and storage conditions. The package contains 30 capsules and displays the NDC number 43386-660-03.*
FDA Label Image

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Label for Trimethobenzamide Hydrochloride Capsules, USP 300 mg by Lupin Pharmaceuticals, Inc. The label displays the active ingredient strength, 300 mg, and package quantity of 100 capsules. It includes dosage information, storage instructions, manufacturer details, and a barcode. The NDC number 43386-660-24 is shown.*
FDA Label Image

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Label for Trimethobenzamide Hydrochloride Capsules, USP 300 mg by Lupin Pharmaceuticals, Inc. Displays NDC 43386-660-26 and specifies 500 capsules per container. Includes dosage form as capsules, oral route, usual adult dosage guidance, storage instructions, and manufacturer details. Label emphasizes prescription-only status.*

* 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.