Diphenoxylate Hydrochloride And Atropine Sulfate Tablet
Product Images NDC 50090-5592

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 Diphenoxylate Hydrochloride And Atropine Sulfate (NDC 50090-5592). 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.

Product Images & Figures Index

FDA Label Image

Chemicalstructureatropine (Chemstructure 01)

Chemicalstructureatropine (Chemstructure 01)
Chemical structure diagram depicting diphenoxylate hydrochloride and atropine sulfate. The drawing includes molecular bonds and groups, with a notation indicating the presence of sulfuric acid and water molecules as part of the sulfate hydrate.*
FDA Label Image

Chemicalstructurediphen (Chemstructure)

Chemicalstructurediphen (Chemstructure)
Chemical structure of diphenoxylate hydrochloride as shown in the image, illustrating the molecular connections and groups including a piperidine ring, ester functional group, nitrile group, and hydrochloride salt.*
FDA Label Image

Label Image (Lbl500905592)

Label Image (Lbl500905592)
Label for Diphenoxylate Hydrochloride and Atropine Sulfate 2.5 mg / 0.025 mg oral tablets by A-S Medication Solutions. The label states the package contains 20 tablets and includes warnings such as storage below 77°F, habit-forming potential, and restriction to prescription use only (RX ONLY). It also includes the product's National Drug Code (NDC) 50090-5592-0 and packaging information.*

* 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.