Bloxiverz
Product Images NDC 51754-1240

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bloxiverz (NDC 51754-1240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Exela Pharma Sciences, 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

Structural Formula Of Neostigmine Methylsulfate (Bloxiverz Novaplus 01)

Chemical structure of Bloxiverz, depicting the molecular arrangement including a quaternary ammonium group, methanesulfonate, aromatic ring, and amide functionalities, consistent with its active ingredient.*

FDA Label Image

1 mg Vial (Image 01)

Label for Bloxiverz (Neostigmine Methylsulfate Injection, USP) by Exela Pharma Sciences, LLC. The vial contains 10 mg/10 mL (1 mg/mL) and is for intravenous use. The label includes storage instructions, preservative information, and a barcode. It states the product is a 10 mL multiple-dose vial.*

FDA Label Image

1 mg Carton (Image 02)

Packaging label for Bloxiverz (Neostigmine Methylsulfate Injection, USP) for intravenous use, 10 mg/10 mL (1 mg/mL) multiple-dose vial. The label includes dosing information, storage instructions, ingredients, and manufacturer details by Exela Pharma Sciences, LLC. The package is marked with the product NDC 51754-1240-1 and the Novaplus logo.*

FDA Label Image

Extended Content Label (Image 03)

Label for Bloxiverz (Neostigmine Methylsulfate Injection, USP) by Exela Pharma Sciences, LLC. This label shows the product strength as 10 mg/10 mL (1 mg/mL) for intravenous use, packaged in 10 x 10 mL multiple-dose vials. The label includes storage instructions, barcode, and ingredient details including preservatives.*

* 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.