Brivaracetam Injection
Product Images NDC 42571-370

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Brivaracetam (NDC 42571-370). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Micro Labs Limited, 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

Brivaracetam-ctn.jpg (Brivaracetam Ctn)

Brivaracetam Injection 50 mg/5 mL (10 mg/mL) intravenous injection packaging label for 10 single-dose 5 mL vials. The label includes storage instructions, inactive ingredients, Rx only designation, and manufacturer details for Micro Labs Limited, India, with distribution by Micro Labs USA, Inc.*

FDA Label Image

Brivaracetam-fig.jpg (Brivaracetam Fig)

A bar chart comparing proportions of patients achieving various percentages of reduction in seizure frequency from baseline across four groups: Placebo, Brivaracetam 50 mg/day, 100 mg/day, and 200 mg/day. The x-axis shows categories of seizure frequency reduction percentages, and the y-axis shows the proportion of patients as a percentage.*

FDA Label Image

Brivaracetam-lbl.jpg (Brivaracetam Lbl)

Label for Brivaracetam Injection 50 mg/5 mL (10 mg/mL) intravenous injection, 5 mL single-dose vial by Micro Labs Limited. The label includes usage instructions for intravenous use only, discard unused portion, and notes it is Rx only. The NDC is 42571-370-92.*

FDA Label Image

Brivaracetam-structure.jpg (Brivaracetam Structure)

Chemical structure of Brivaracetam showing its molecular framework with a pyrrolidinone ring, including stereochemistry and functional groups consistent with the active ingredient.*

* 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.