Glycopyrrolate Injection
Product Images NDC 71872-7012

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 71872-7012). 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

Vial (20ml Vial)

Vial (20ml Vial)
Glycopyrrolate Injection USP 4 mg/20 mL (0.2 mg/mL) vial label for intramuscular or intravenous use. Contains benzyl alcohol as preservative. The vial is a 20 mL multiple-dose container labeled for prescription use only. Manufactured by Vintax Limited, Bangalore, India, and for Sequent Therapeutics LLC, Mendham, NJ. Storage instructions and barcode are present, with a note indicating it is not for use in newborns.*
FDA Label Image

Molecular Structure (3f3b363b Fe6d 4dee 89bd C2ca992dcf49 01)

Molecular Structure (3f3b363b Fe6d 4dee 89bd C2ca992dcf49 01)
Chemical structure of glycopyrrolate, depicting its molecular formula C19H28BrNO3 and molecular weight of 398.33.*
FDA Label Image

Pdp (7012)

Pdp (7012)
Label for Glycopyrrolate Injection, USP, 0.2 mg/mL (4 mg/20 mL) multiple-dose vial for intramuscular or intravenous use. The label includes storage instructions (20°-25°C), manufacturer information (Wintac Limited, India; Somerset Therapeutics LLC, NJ), repackaged and distributed by Medical Purchasing Solutions, Scottsdale, AZ, and warnings such as not for use in newborns and presence of benzyl alcohol preservative.*

* 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.