Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 51655-322

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 51655-322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

51655-322-25 (51655 322 25 Rev A 04 23)

51655-322-25 (51655 322 25   Rev A 04 23)
Label for Labetalol Hydrochloride Tablets USP 100 mg, containing 60 film-coated tablets. The label notes prescription only use and storage instructions at 20°-25°C. It is repackaged by Northwind Pharmaceuticals in Indianapolis, IN. The label includes NDC 51655-322-25 and additional batch and packaging details.*
FDA Label Image

Chem Structure (Chemstructure)

Chem Structure (Chemstructure)
Chemical structure of Labetalol Hydrochloride showing the molecular arrangement and the molecular formula C19H24N2O3·HCl with molecular weight 364.87.*

* 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.