Clomipramine Hydrochloride Capsule
Product Images NDC 68180-494

View Photos of 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 Clomipramine Hydrochloride (NDC 68180-494). 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 Clomipramine Hydrochloride showing its molecular arrangement including the tricyclic ring system with chlorine atom and the dimethylaminopropyl side chain, accompanied by a hydrochloride group.*
FDA Label Image

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Label for Clomipramine Hydrochloride Capsules USP 25 mg by Lupin Pharmaceuticals, Inc. The label states it contains 30 capsules with NDC 68180-492-06. It includes storage instructions, a barcode, and manufacturing details for Lupin Pharmaceuticals in the USA and Lupin Limited in India. The label emphasizes pharmacist dispensing with a medication guide.*
FDA Label Image

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Label for Clomipramine Hydrochloride Capsules USP 50 mg by Lupin Pharmaceuticals, Inc. The label states it contains 30 capsules and is for oral use. It includes directions for pharmacists to dispense with a medication guide and storage instructions. Manufacturing information lists Lupin Pharmaceuticals in Baltimore, MD, and Lupin Limited in Nagpur, India.*
FDA Label Image

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Label for Clomipramine Hydrochloride Capsules USP 75 mg by Lupin Pharmaceuticals, Inc. The label indicates 30 capsules per container, prescription only, with storage instructions and manufacturer information including Lupin Limited in India.*

* 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.