Benazepril Hydrochloride Tablet, Coated
Product Images NDC 70518-2125

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride (NDC 70518-2125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Benazepril HCl 40mg 70518 2125 01

Benazepril HCI is a prescription medication with NDC number 70518-2125-01, manufactured by Sclco in Cranbury, NJ 08512. It should be kept out of reach of children and stored between 20-26°C (63-77°F), with excursions permitted up to 15-30°C (59-86°F). This medication should be used as directed in the package insert. The lot number and expiry date are not available. It has been repackaged by RemedyRepack Inc. in Indiana, PA 15701.*

FDA Label Image

Remedy_label (Remedy Label)

Benazepril HCI is a prescription medication repackaged by RemedyRepack Inc., Indiana, PA. The manufacturer is Sclco of Cranbury, NJ. The medication must be kept out of reach of children and should be stored at a temperature between 20-26°C (63-77°F), with excursions allowed to 15-30°C (59-86°F) [see USP]. The NDC # for this medication is 70518-2125-00 and the source NDC is 43547-0338-50. Expiration date and lot # are not available. Please refer to the package insert for usage instructions.*

FDA Label Image

Structure (Bb91223e Ffa5 4a3a B191 Fe121250c20c 01)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.