Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 71335-9690

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 71335-9690). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

The Following Structure For Labetalol Hydrochloride, Usp Is A Racemate, Chemically Designated As 2-hydroxy-5-[1-hydroxy-2-[(1-methyl-3-phenylpropyl)amino]ethyl] Benzamide Monohydrochloride. (Labetalol HCl Tablets 01)

Chemical structure of labetalol hydrochloride showing the molecular arrangement including phenyl groups, hydroxyl, amine, and amide functional groups with an associated hydrochloride ion.*

FDA Label Image

Label (Lbl713359690)

Label for Labetalol Hydrochloride Tablets, USP 300 mg, film-coated oral tablets. The label states the package contains 30 tablets and is repackaged by Bryant Ranch Prepack, Inc. in Burbank, CA, and manufactured by Method Pharmaceuticals LLC. Storage instructions and standard warnings about keeping drugs out of reach of children are included. The NDC code is 71335-9690-1.*

* 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.