Glycopyrrolate
Product Images NDC 71872-7227

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 Glycopyrrolate (NDC 71872-7227). 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

1-ml-vial-label.jpg (1 mL Vial Label)

1-ml-vial-label.jpg (1 mL Vial Label)
Label for Glycopyrrolate Injection, USP 0.2 mg/mL in a 1 mL single dose vial. The label indicates it contains benzyl alcohol and is for intramuscular or intravenous use. Manufactured by Indoco Remedies Limited and labeled for Apotex Corp.*
FDA Label Image

71872-7227-1.pdp (71872 7227 1)

71872-7227-1.pdp (71872 7227 1)
Glycopyrrolate Injection, USP 0.2 mg/mL (0.2 mg) 1 mL single-dose vial label. The label states quantity as 1 vial, includes lot and expiration placeholders, and warns against use in newborns. It lists ingredients including benzyl alcohol and water for injection with pH adjustment, storage instructions (20°C to 25°C, excursions permitted 15°C to 30°C), and dosage direction to see package insert. Manufactured by Indoco Remedies Limited, India, repackaged and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ.*
FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of glycopyrrolate showing the two isomeric forms with molecular formula C19H28BrNO3 and molecular weight 398.33 g/mol. The structure includes ester and quaternary ammonium groups with bromide counterions.*

* 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.