Amlodipine Besylate And Benazepril Hydrochloride
Product Images NDC 68151-1365

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate And Benazepril Hydrochloride (NDC 68151-1365). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carilion Materials Management, 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 Image (68151 1365)

Label Image (68151 1365)
Label of Amlodipine Besylate and Benazepril Hydrochloride capsules, showing strength 5 mg/20 mg. The label includes manufacturer Lupin Ltd., lot number H400540, expiration date 10/14, product NDC 68151-1365, and indicates prescription only. A barcode with the number 0000001365 is also visible.*
FDA Label Image

Benazepril Hydrochloride Structural Formula (Amlodipine Besylate And Benazepril Hydrochloride 01)

Benazepril Hydrochloride Structural Formula (Amlodipine Besylate And Benazepril Hydrochloride 01)
Chemical structure of the active ingredient benazepril hydrochloride, showing its molecular framework with labeled functional groups and the hydrochloride salt component.*
FDA Label Image

Amlodipine Besylate Structural Formula (Amlodipine Besylate And Benazepril Hydrochloride 02)

Amlodipine Besylate Structural Formula (Amlodipine Besylate And Benazepril Hydrochloride 02)
Chemical structure of Amlodipine Besylate and Benazepril Hydrochloride active ingredients, showing molecular diagrams including aromatic rings, chlorine, sulfur groups, and ester and amine functional groups.*

* 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.