Benazepril Hydrochloride Tablet, Coated
Product Images NDC 68788-9313

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride (NDC 68788-9313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred 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

Structure (Bb91223e Ffa5 4a3a B191 Fe121250c20c 01)

Chemical structure diagram of Benazepril Hydrochloride, showing its molecular framework with labeled functional groups and the hydrochloride component.*

FDA Label Image

Benazepril Hydrochloride Tabler 10mg (Bb91223e Ffa5 4a3a B191 Fe121250c20c 03)

Label for Benazepril Hydrochloride Tablet 10 mg, a coated oral tablet. The label shows the generic name, strength, and that it is generic for Lotensin. It includes manufacturer details for Solco Healthcare U.S., LLC in Cranbury, NJ, and states storage instructions at controlled room temperature. The label features dosing directions in English and Spanish, with spaces to fill tablet count and hours between doses. The label is from Preferred Pharmaceuticals, Inc.*

FDA Label Image

Benazepril Hydrochloride Tabler 20mg (Bb91223e Ffa5 4a3a B191 Fe121250c20c 04)

Label for Benazepril Hydrochloride Tablet 20 mg, coated tablets for oral use, generic for Lotensin. The label shows the product strength (20 mg), manufacturer as Solco Healthcare U.S., LLC, and storage instructions. Directions for use are printed in English and Spanish on a yellow background. The label includes spaces for lot number, batch number, expiration date, and insurance information but they are blank.*

* 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.