Vancomycin Hydrochloride
Product Images NDC 45932-0029

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 45932-0029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xellia Pharmaceuticals, Aps, 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

1g (Vancomycin Carton 1g)

The text appears to be a pharmaceutical label for Vancomycin Hydrochloride for Injection, USP. It includes dosage instructions, precautions and manufacturer details. It also mentions the need for dilution and storage conditions.*

FDA Label Image

500mg (Vancomycin Carton 500mg)

The text is a description of a medicine named Vancomycin Hydrochloride for Injection, USP. It comes in a sterile, lyophilized form contained in a vial of 500mg/vial. Dilute the content of the vial with 10 mL Sterile Water for Injection before use. The text also mentions that it is important to read the insert for precautions and directions before use. The usual adult dosage is 2 daily in divided doses. The medicine should be refrigerated for 96 hours without significant loss of potency.*

FDA Label Image

1g (Vancomycin Container 1g)

NDC 45932-0029-1 is a prescription drug used for intravenous injection in adults usually divided into 2 doses of 2 grams daily after reconstitution. The drug comes in sterile, lyophilized form in a vial containing Vancomycin Hydrochloride equivalent to 1 g. The vial must be diluted with 20 mL sterile water for injection before use and stored in the refrigerator for 96 hours post-reconstitution. The insert should be read for precautions and directions before use. The drug is manufactured in Denmark by Xellia Pharmaceuticals ApS.*

FDA Label Image

500mg (Vancomycin Container 500g)

Vancomycin Hydrochloride for Injection is a sterile, lyophilized injection used for intravenous use. Each vial contains Vancomycin Hydrochloride equivalent to 500mg Vancomycin. It must be further diluted before use, and precautions and directions must be read before use. The usual adult dosage is 2g daily in divided doses. The contents of the vial must be diluted with 10mL of sterile water for injection. Prior to reconstitution, it must be stored at 20° to 25°C (68° to 77°F) and after reconstitution, it can be stored in the refrigerator for 96 hours without significant loss of potency. Made in Denmark by Xellia Pharmaceuticals ApS.*

FDA Label Image

Des (Vancomycin Description)

FDA Label Image

1 Gram (Vancomycin Tray 1g)

This appears to be a product insert for an injectable medication called Vancomycin Hydrochloride. It contains instructions for use, dosage information, and warnings. The medication is supplied as a powder in a vial that must be mixed with sterile water prior to use. It should be stored at controlled room temperature or refrigerated after reconstitution. The manufacturer is listed as Xlia Pharmaceutcas ApS in Denmark.*

FDA Label Image

500mg (Vancomycin Tray 500mg)

Vancomycin Hydrochloride is an injectable antibiotic medication used to treat bacterial infections. It is available in vials containing 10500 mg of the drug and must be diluted prior to administration. Patients are instructed to read the insert for precautions before usage. Other information regarding dosage and storage recommendations are included on the label. The provided text contains some unclear and potentially corrupted characters, but the text does not appear to contain useful information on usage or storage beyond these details.*

FDA Label Image

Logo (Vancomycin Xellialogo)

* 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.