Metoprolol Injection
Product Images NDC 36000-033

3 FDA label images from Baxter Healthcare Corporation · 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 (NDC 36000-033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Structural-formula-metoprolol (Structural Formula Metoprolol)

Structural-formula-metoprolol (Structural Formula Metoprolol)
Chemical structure diagram depicting the molecular composition of metoprolol tartrate, including labeled functional groups and atomic arrangements consistent with the active ingredient in the Metoprolol injection product.*
FDA Label Image

5mg-5ml-container-label (5mg 5ml Container Label)

5mg-5ml-container-label (5mg 5ml Container Label)
Label for Metoprolol Tartrate Injection, USP 5 mg/5 mL (1 mg/mL) intravenous sterile single dose vial by Baxter Healthcare Corporation. The label includes active ingredient information, usage route, barcode, lot number, and manufacturing details from Baxter Pharmaceuticals India Private Ltd.*
FDA Label Image

5mg-5ml-carton-label (5mg 5ml Carton Label)

5mg-5ml-carton-label (5mg 5ml Carton Label)
Packaging label for Metoprolol Tartrate Injection, USP 5 mg/5 mL (1 mg/mL) intravenous injection by Baxter Healthcare Corporation. The label indicates 10 sterile single dose vials of 5 mL each, manufactured by Baxter Pharmaceuticals India Private Ltd. Storage instructions and NDC 36000-033-10 barcode are visible.*

* 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.