Imipramine Hydrochloride
Product Images NDC 64125-134

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Imipramine Hydrochloride (NDC 64125-134). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Excellium Pharmaceutical, 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

Imipramine 10mg 100tab Label (Imipramine 10mg 100tab)

Imipramine Hydrochloride Tablets, USP 10 mg, prescription medication by Excellium Pharmaceutical, Inc. The label indicates a package containing 100 tablets. Features include dosage strength, NDC number 64125-133-01, storage instructions, and warnings to keep out of reach of children.*

FDA Label Image

Imipramine 25mg 100tab Label (Imipramine 25mg 100tab)

Imipramine Hydrochloride Tablets, USP 25 mg, in a bottle label format from Excellium Pharmaceutical, Inc. The label indicates a prescription-only medication with a count of 100 tablets. It includes storage instructions, bar code, and safety warnings to keep out of reach of children.*

FDA Label Image

Imipramine 50mg 100tab Label (Imipramine 50mg 100tab)

Imipramine Hydrochloride Tablets, USP 50 mg bottle label from Excellium Pharmaceutical, Inc. The label indicates 100 tablets, prescription only, with directions to keep out of reach of children. It includes storage instructions and a barcode with the NDC 64125-135-01.*

FDA Label Image

Chemical Structure (Imipramine Structure)

Chemical structure of Imipramine Hydrochloride, showing the molecular arrangement including nitrogen atoms, aromatic rings, a methyl group, and a hydrochloride component.*

* 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.