Glycopyrrolate Injection
Product Images NDC 86211-113

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 86211-113). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jvet Pharmaceuticals 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

Carton (Carton)

Carton (Carton)
Glycopyrrolate Injection, USP 4 mg/20 mL (0.2 mg/mL) injection carton label by JPharma, indicating human prescription drug for intramuscular or intravenous administration. The label includes warnings such as 'NOT FOR USE IN NEWBORNS' and states the product contains benzyl alcohol. The package contains 10 multiple dose vials of 20 mL each.*
FDA Label Image

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

Glycopyrrolate-spl-structural-formula (Glycopyrrolate Spl Structural Formula)
Chemical structure of glycopyrrolate, showing the molecular formula C19H28BrNO3 and molecular weight 398.33. The structure includes a quaternary ammonium group with bromide counterion.*
FDA Label Image

Label (Label)

Label (Label)
Label for Glycopyrrolate Injection, USP 4 mg/20 mL (0.2 mg/mL) by Jvet Pharmaceuticals LLC. The label indicates the product is for intramuscular or intravenous administration, contains benzyl alcohol, and is supplied as a 20 mL multiple dose vial. Storage instructions specify 20°C to 25°C (68°F to 77°F). The label includes dosing instructions note and barcode.*

* 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.