Verapamil Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 51655-956

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Verapamil Hydrochloride (NDC 51655-956). 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

Verapamil HCl 51655-956 (Verapamil HCl 51655 956)

Label for verapamil hydrochloride extended release tablets, 240 mg strength, oral route. The label states the package contains 30 film-coated tablets, prescription only, with lot number NW08220001 and expiration date 02/2016. The manufacturer is Glenmark Generics Ltd., India, for Glenmark Generics Inc., NJ, USA, and repackaged by Northwind Pharmaceuticals, Indianapolis, IN. The label includes storage instructions and dosage form details.*

* 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.