Glycopyrrolate Injection
Product Images NDC 71872-7224

3 FDA label images from Medical Purchasing Solutions, Llc · 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 71872-7224). 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

71872-7224-1.pdp (71872 7224 1)

71872-7224-1.pdp (71872 7224 1)
Glycopyrrolate Injection, USP 0.2 mg/mL in a 1 mL single dose vial. The label states the product is for intramuscular or intravenous administration and contains benzyl alcohol as a preservative. It is manufactured for Airomed, LLC and repackaged and distributed by Medical Purchasing Solutions, LLC. Storage instructions specify 20° to 25°C (68° to 77°F).*
FDA Label Image

Glycopyrrolate-spl-1ml-container-label (Glycopyrrolate Spl 1ml Container Label)

Glycopyrrolate-spl-1ml-container-label (Glycopyrrolate Spl 1ml Container Label)
Label for Glycopyrrolate Injection, USP 0.2 mg/mL, a 1 mL single dose vial for intramuscular or intravenous use. Contains Benzyl Alcohol. The label shows storage instructions, a barcode, and manufacturer information for Xiromed, LLC. NDC is partially visible.*
FDA Label Image

Glycopyrrolate-spl-structural-formula (Glycopyrrolate Spl Structural Formula)

Glycopyrrolate-spl-structural-formula (Glycopyrrolate Spl Structural Formula)
Chemical structure of glycopyrrolate, showing its molecular composition including a pyrrolidinium ring and aromatic group. The molecular formula (C19H28BrNO3) and molecular weight (398.33) are indicated below the structure.*

* 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.