Labetalol Hydrochloride Injection
Product Images NDC 83301-0058

View Photos of 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 Labetalol Hydrochloride (NDC 83301-0058). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mullan Pharmaceutical Inc., 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

Chemical Structure (Labetalol 01)

Chemical Structure (Labetalol 01)
Chemical structure of Labetalol Hydrochloride. The diagram shows the molecular arrangement including benzene rings, hydroxyl groups, amide group, and hydrochloride association consistent with the chemical formula of the compound.*
FDA Label Image

Principal Display Panel (20 mL Vial Carton)

Principal Display Panel (20 mL Vial Carton)
Packaging label for Labetalol Hydrochloride Injection, USP 100 mg/20 mL (5 mg/mL) intravenous injection. The label indicates a 20 mL multiple-dose vial, manufactured for Mullan Pharmaceutical Inc., Pasadena, CA, and by Gland Pharma Limited, Hyderabad, India. The label includes storage instructions, preservative information, and batch/barcode areas, with Mullan branding displayed prominently.*
FDA Label Image

Principal Display Panel (40 mL Vial Carton)

Principal Display Panel (40 mL Vial Carton)
Packaging label for Labetalol Hydrochloride Injection, USP 200 mg/40 mL (5 mg/mL) intravenous injection by Mullan Pharmaceutical Inc. The label describes a 40 mL multiple-dose vial and includes storage instructions, manufacturer information, and dosage concentration details. The design features a magenta label panel with white text and the Mullan logo at the bottom.*

* 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.