Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 51655-213

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amlodipine And Benazepril Hydrochloride (NDC 51655-213). 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

Label (51655 213 26)

Label (51655 213 26)
Label for Amlodipine and Benazepril Hydrochloride Capsules, USP, 10 mg/20 mg, containing 90 capsules in the package. The label includes storage instructions, dosage reference to package insert, and identification information for Northwind Pharmaceuticals and Northwind Health Company, LLC, the repackager and labeler. Additional details include color additive information and stability storage temperature.*
FDA Label Image

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)
Chemical structure of Amlodipine and Benazepril Hydrochloride, showing the molecular arrangement including aromatic rings, functional groups, and the presence of hydrochloride (HCl).*
FDA Label Image

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)
Chemical structure diagrams of components related to the Amlodipine and Benazepril Hydrochloride product, showing molecular arrangements with various functional groups including a chlorine atom and a sulfonic acid group.*

* 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.