Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 72789-412

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 72789-412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789412 Label (72789412)

72789412 Label (72789412)
This is a pharmaceutical label containing information about a medication called amLODIPine/BENAZEPRIL in the form of capsules. It provides details such as the dosage strength (10MG/20 MG), the number of capsules (90), and instructions for taking them. The label also includes a caution to discontinue use if pregnancy is detected and mentions to seek medical advice about side effects. The expiration date of the medication is 07/2025, and it is equivalent to amLODIPINE 10 MG AND BENAZEPRIL HYDROCHLORIDE USP 20 MG.*
FDA Label Image

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)

FDA Label Image

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)

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