Amlodipine Besylate And Benazepril Hydrochloride Capsule
Product Images NDC 55111-586

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate And Benazepril Hydrochloride (NDC 55111-586). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories Limited, 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

Container1 (Container1)

Label for Amlodipine and Benazepril Hydrochloride Capsules, USP 5 mg/40 mg by Dr. Reddy's Laboratories Limited. The label states the product contains 100 capsules and is for prescription use only. It includes dosing information, storage instructions, a barcode, a QR code for patient information, and a pharmacist dispensing note.*

FDA Label Image

Container2 (Container2)

Label for Amlodipine and Benazepril Hydrochloride Capsules, USP 10 mg/40 mg, in a 100 capsule bottle. The label includes instructions to dispense with patient information sheet, manufacturer Dr. Reddy's Laboratories Limited, and a QR code for patient information. The label also lists active ingredients per capsule and storage instructions.*

FDA Label Image

Structure01 (Structure01)

Chemical structure of Benazepril Hydrochloride, one of the active ingredients in Amlodipine Besylate and Benazepril Hydrochloride capsules by Dr. Reddy's Laboratories Limited.*

FDA Label Image

Structure02 (Structure02)

Chemical structure diagram showing the molecular structure of an active ingredient related to Amlodipine Besylate and Benazepril Hydrochloride. The diagram includes labeled atoms and functional groups linked by chemical bonds.*

* 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.