Benazepril Hydrochloride Tablet, Film Coated
Product Images NDC 51655-388

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride (NDC 51655-388). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

51655-388-52 (51655 388 52 Rev A 05 23)

51655-388-52 (51655 388 52   Rev A 05 23)
NDC: 51655-388-52 is the identifier for Benazepril Hydrochloride Tablets, USP with a strength of 20mg and a package size of 30 tablets. This medication is available only with a prescription. The recommended dosage information can be found in the package insert. It is advised to store this medication at a temperature between 20°C to 25°C (68°F to 77°F), with temporary excursions allowed between 15°C to 30°C (59°F to 86°F). Keep the medication out of reach of children and store it in its original container, protected from moisture. The manufacturer is Aurobindo Pharma USA, Inc., and it has been repackaged by Northwind Pharmaceuticals. The product can be identified with the GTIN number: 00351655388525. The lot and expiration dates are both marked as 0000000000.*
FDA Label Image

Chemical Structure (Benazepril Str)

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