Imipramine Hydrochloride Tablet, Film Coated
Product Images NDC 80425-0294

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Imipramine Hydrochloride (NDC 80425-0294). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, Llc, 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

Description (Description)

Chemical structure diagram of Imipramine hydrochloride showing its molecular arrangement, including aromatic rings and side chains, with the presence of HCl indicating the hydrochloride form.*

FDA Label Image

Label 1 (Impiramine 10mg 80425 0294 01)

Imipramine HCl 10 mg film-coated tablet label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions (20-25°C), lot number, expiration date (12/31/2023), and comparison information to TOFRANIL with corresponding NDC codes.*

FDA Label Image

Label 2 (Impiramine 10mg 80425 0294 02)

Imipramine hydrochloride 10 mg film-coated tablets label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions (20-25°C), a comparison to Tofranil, and package quantity (#60). It also displays NDC 80425-0294 and expiration date 12/31/2023, with an alternate label from Leading Pharma shown in part.*

FDA Label Image

Label 3 (Impiramine 10mg 80425 0294 03)

Imipramine hydrochloride 10 mg film-coated tablets packaging label. The label includes the proprietary and generic names, strength, tablet form, and labeler information for Advanced Rx Pharmacy of Tennessee, LLC. It also lists NDC numbers, lot number, and expiration date, along with storage instructions (20-25°C) and a comparison to the brand Tofranil.*

* 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.