Verapamil Hydrochloride Injection, Solution
Product Images NDC 51662-1685

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Verapamil Hydrochloride (NDC 51662-1685). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Structure (51662 1685 Structure)

Chemical structure of verapamil hydrochloride showing its molecular configuration including aromatic rings, methoxy groups, and isopropyl side chains, along with the hydrochloride component.*

FDA Label Image

Table (51662 1685 Table 1)

Table titled 'Suggested Treatment of Acute Cardiovascular Adverse Reactions' listing adverse reactions, their proven effective treatments, and supportive treatments. Examples include symptomatic hypotension treated with dopamine, calcium chloride, norepinephrine bitartrate, metaraminol bitartrate, or isoproterenol HCl intravenously, supported by intravenous fluids and Trendelenburg position. Bradycardia and AV block treatments include isoproterenol HCl, calcium chloride, norepinephrine bitartrate, atropine, and cardiac pacing, with slow drip intravenous fluids as support. Rapid ventricular rate treatments involve DC-cardioversion, procainamide, and lidocaine intravenously, also supported by slow drip intravenous fluids.*

FDA Label Image

Label (51662 1685 1 Rfidlabel)

A product label for VERAPAMIL HYDROCHLORIDE injection, solution, distributed by HF Acquisition Co., LLC in Mukilteo, WA. It includes barcode data strings and a note to see the manufacturer's insert. The label indicates the product is for prescription use only (RX ONLY).*

* 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.