Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 72789-285

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 72789-285). 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

72789285 Label (72789285)

Each capsule contains 13.9 mg of Amlodipine Besylate USP equivalent to Amlodipine 10 mg and Benazepril Hydrochloride USP 20 mg, indicated for hypertension treatment. It contains FD&C Yellow N5 (Tartrazine) as a color additive, must be kept in a tight container, and stored at 20-25°C (68-77°F) with excursions permitted to 15° to 30°C (50° 1 B6°F) [Se USP Controlled Room Temperature]. Dispensed by a doctor’s prescription and kept out of reach of children. The medication is manufactured and imported from Hyderabad-500 038, India. Expired on September 2023, with LOT: G22F82.*

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.