4d517ecd-figure-01 (Glycopyrrolate Injection Civica 1)
Glycopyrrolate Injection, Solution
Product Images NDC 72572-226
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Glycopyrrolate (NDC 72572-226). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Civica, 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.
Civica Logo (Glycopyrrolate Injection Civica 2)
Vial Label Civica (Glycopyrrolate Injection Civica 3)
NDC 72572-226-01 is a prescription drug that should only be used for IM or IV purposes, as indicated in the package insert. The manufacturer is Civica, Inc, and the drug should be stored between 20 to 25°C. The drug comes in 1 mL single-dose vials with a strength of 0.2 mg/mL, and any unused portions should be discarded. The drug is Glycopyrrolate Injection, USP, and can only be used under the guidance of a healthcare professional.*
Box Label (civica) (Glycopyrrolate Injection Civica 4)
Glycopyrrolate Injection, USP with a concentration of 0.2 mg/mL is intended for intramuscular or intravenous use. The solution contains Glycopyrrolate 0.2 mg, Benzyl Alcohol 0.9%, Water for Injection q.s. The pH is adjusted with Sodium Hydroxide and/or Hydrochloric Acid. The warning statement indicates that the unused portion should be discarded. The product is available in 25X 1 mL single-dose vials. The medication should be stored at a temperature of 20°C to 25°C. The package insert should be used for reference. The medicine is manufactured by American Regent, Inc. for Civica, Inc. The lot number and expiration date are specified.*
Serialization Label (Glycopyrrolate Injection Civica 5)
* 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.
