Metoprolol Tartrate Injection, Solution
Product Images NDC 71872-7226

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 Metoprolol Tartrate (NDC 71872-7226). 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.

FDA Label Image

71872-7226-1.pdp (71872 7226 1)

71872-7226-1.pdp (71872 7226 1)
Metoprolol Tartrate Injection, USP 1 mg/mL (5 mg/5 mL) single-dose vial label. It states the vial contains 5 mL for intravenous use, includes storage instructions between 20°C to 25°C, protection from light, and warnings not to freeze. Manufactured by Gland Pharma Limited, India, distributed by Almacjet Inc., NJ, and Medical Purchasing Solutions, Scottsdale, AZ. The label also notes the lot number, expiration date placeholders, and detailed product components.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram showing metoprolol tartrate, the active ingredient as indicated by the product data. The structure includes the metoprolol molecule and the tartrate moiety, depicted with molecular bonds and functional groups.*
FDA Label Image

Vial-label (Vial Label)

Vial-label (Vial Label)
Label for Metoprolol Tartrate Injection, USP 5 mg/5 mL (1 mg/mL) intravenous solution in a 5 mL single-dose vial. The label includes storage instructions, manufacturer details for Almaject, Inc., and specifies sterile use and prescription only. The label also features a barcode and batch information area.*

* 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.