Methscopolamine Bromide Tablet
Product Images NDC 51991-191

3 FDA label images from Breckenridge Pharmaceutical, Inc. · 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 Methscopolamine Bromide (NDC 51991-191). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Breckenridge Pharmaceutical, Inc., 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

Chemical Structure (Methscopolamine 01)

Chemical Structure (Methscopolamine 01)
Chemical structure diagram of methscopolamine bromide, a compound showing its molecular arrangement including phenyl, hydroxyl, ester, and quaternary ammonium groups with the bromide anion.*
FDA Label Image

Principal Display Panel (2.5 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg Tablet Bottle Label)
Methscopolamine Bromide Tablets 2.5 mg oral tablets label showing active ingredient strength, inactive ingredients, storage instructions, and warnings. The label includes the NDC number 51991-191-01, manufacturer and distributor information by Breckenridge Pharmaceutical, Inc. The package contains 100 tablets and includes a barcode.*
FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Principal Display Panel (5 mg Tablet Bottle Label)
Label for Methscopolamine Bromide Tablets 5 mg by Breckenridge Pharmaceutical, Inc. The oral tablets packaging states each tablet contains 5 mg of methscopolamine bromide. The label includes inactive ingredients, storage instructions, barcode, and manufacturing information by LGM Pharma Solutions, LLC.*

* 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.