Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 50090-4284

3 FDA label images from A-s Medication Solutions · 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 50090-4284). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)
Chemical structure of Amlodipine and Benazepril Hydrochloride shown as a detailed molecular diagram with labeled bonds and atoms, including a phenyl group and hydrochloride (HCl) component.*
FDA Label Image

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)
Chemical structure diagram showing two molecular structures. The larger structure includes symbols such as Cl, CO2CH2CH3, and other groups, likely representing a complex organic molecule. The smaller structure appears as a simpler aromatic ring with a SO3H group attached, indicative of a sulfonic acid derivative.*
FDA Label Image

Label Image (Lbl500904284)

Label Image (Lbl500904284)
The label for Amlodipine and Benazepril Hydrochloride 5 mg / 20 mg capsules from A-S Medication Solutions. It indicates each capsule contains amlodipine besylate equivalent to 5 mg amlodipine and 20 mg benazepril hydrochloride USP. The label advises storage below 77 degrees Fahrenheit and notes a package size of 30 capsules.*

* 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.