Esmolol Hydrochloride Injection
Product Images NDC 71872-7136

3 FDA label images from Medical Purchasing Solutions, Llc · 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 Esmolol Hydrochloride (NDC 71872-7136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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.

Product Images & Figures Index

FDA Label Image

Pdp (7136)

Pdp (7136)
Label for Esmolol Hydrochloride Injection 10 mg/mL single dose vial. The label shows the product name, concentration, quantity (1 vial), lot number and expiration date placeholders, and states it contains no preservatives and is for intravenous use. It includes storage instructions, manufacturer Baxter Healthcare Corporation, repackager Medical Purchasing Solutions, and contact information.*
FDA Label Image

Esmolol Hydrochloride Structural Formula (Image 01)

Esmolol Hydrochloride Structural Formula (Image 01)
Chemical structure of Esmolol Hydrochloride, showing its molecular arrangement including aromatic ring and functional groups as part of the hydrochloride salt form.*
FDA Label Image

Esmolol Container Label (Image 02)

Esmolol Container Label (Image 02)
Label of Esmolol Hydrochloride Injection 100 mg/10 mL (10 mg/mL) intravenous injection in a 10 mL ready-to-use vial. The label indicates it is for intravenous use only, preservative-free, iso-osmotic, and includes manufacturer information: Baxter Healthcare Corporation, Deerfield, IL, USA. The label also features NDC 10019-120-39 and a barcode.*

* 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.