Labetalol Hydrochloride Injection
Product Images NDC 72266-102

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 72266-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fosun Pharma Usa 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

Labetalol 20ml Label

Label for Labetalol Hydrochloride Injection, USP, 5 mg/mL (100 mg/20 mL) in a 20 mL multi-dose vial. Intended for intravenous injection only, distributed by Fosun Pharma USA Inc., made in India. The label includes ingredient information, storage instructions, and a barcode.*

FDA Label Image

Labetalol 40ml Carton

Packaging label for Labetalol Hydrochloride Injection, USP, 5 mg/mL strength in a 40 mL multi-dose vial. The label states it is for intravenous injection only and is distributed by Fosun Pharma USA Inc. The concentration is 200 mg per 40 mL. The label includes storage instructions and the manufacturer's location, India.*

FDA Label Image

Labetalol 40ml Label

Label for Labetalol Hydrochloride Injection, USP, 5 mg/mL (200 mg/40 mL) in a 40 mL multi-dose vial. The label states it is for intravenous injection only, prescription use, and is distributed by Fosun Pharma USA Inc. It includes storage instructions and mentions the vial is made in India. A barcode and space for lot and expiration dates are also visible.*

FDA Label Image

Labetalol Structural Formula

Chemical structure of Labetalol Hydrochloride showing its molecular components including aromatic rings, hydroxyl groups, amide, and hydrochloride salt.*

FDA Label Image

Labetolol 20ml Carton

Label for Labetalol Hydrochloride Injection USP, 5 mg/mL strength, in a 20 mL multi-dose vial. The label specifies intravenous injection only and includes the NDC 72266-102-01. Distributed by Fosun Pharma USA Inc., Princeton, NJ. The label includes storage instructions and ingredients.*

* 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.