Chemical Structure (Vancomycin 02)
Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 0409-3515
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0409-3515). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hospira, 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.
Product Images & Figures Index
Logo (Vancomycin 03)
Principal Display Panel (750 mg Vial Label)
Vancomycin Hydrochloride for Injection is a sterile powder medicine used for intravenous use only after dilution in sterile water for injection. It is important to read and follow the precautions and directions provided in the insert. It may contain HCI and/or NaOH for pH adjustment. The usual adult dose is 2g daily. After dilution, it must be refrigerated. Prior to reconstitution, it should be stored at a controlled room temperature of 20-25°C. The manufacturer is Hospira, Inc. The Lot and Expiry dates are also provided.*
Principal Display Panel (750 mg Vial Tray)
This is a description of a medication called Vancomycin which is a sterile powder for intravenous use only. The user must further dilute it before use. The instructions and precautions must be read before administration. The medication may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Following reconstitution, it may be stored in a refrigerator for 14 days without significant loss of potency. The medication is distributed by Hospira, Inc. and is available in a 750mg dose.*
Principal Display Panel (1 g Vial Label)
This text describes the usage, dosage, dilution, and storage details of a medication called Vancomycin in sterile powder form. It is for intravenous use only, and must be diluted with sterile water for injection before use. The usual adult dose is 2g daily, and after dilution, it must be refrigerated. The medication is distributed by Hospira, Inc. and must be further diluted according to the insert provided. The text also states that the medication may contain Hydrogen Chloride for injection, and advises reading the insert before use. Finally, the lot number and expiration date are listed.*
Principal Display Panel (1 g Vial Tray)
Vancomycin Hydrochloride for Injection, USP is an antibiotic medication used for intravenous use in hospitals. It is equivalent to 1 Vancomycin gram. The usual adult dose is 2 grams daily and the medication must be diluted before use to avoid significant loss of potency. It needs to be further diluted before use, and the instructions should be followed. This medication is distributed by Hospira, Inc, in Lake Forest, L 60045, USA.*
Principal Display Panel (1 g Vial Carton)
This text seems to be a mix of product information for a Vancomycin Hydrochloride injection for intravenous use, with information on manufacturers and distributors. There is also some illegible text. It provides instructions on dilution before usage and mentions a unique NDC code.*
Principal Display Panel (500 mg Vial Label)
ZEZ Sterile Powder Vancomycin Hydrochloride is a medication used for intravenous use with an adult dosage of 2 g daily. The package must be refrigerated after dilution and contains 500 mg Vancomycin equivalent. The medication should be further diluted before use and the insert must be read for precautions and directions before use. The package may also contain HCI and/or NaOH for pH adjustment. It is produced by Hospira and distributed by Hospit Inc. The lot number is PAA118519 and expiration is DMMMYYYY.*
Principal Display Panel (500 mg Vial Tray)
This is a description for a medication named Vancomycin. The medication is equivalent to 500 mg and is for intravenous use. It is required to be diluted before it can be used. It comes in a package and contains Hydrochloride for Injection, USP. It is important to take necessary precautions and follow directions before use, including proper storage at room temperature. The manufacturer of the medication is Hospira.*
Principal Display Panel (1.5 g Vial Label)
This is a sterile powder of Vancomycin Hydrochloride for Injection, USP, for intravenous use with an equivalency of 15 mg of vancomycin. The product must be further diluted before use and should be refrigerated after dilution. The usual adult dose is 29 daily and should be diluted with 30 mL of Sterile Water for Injection. The product contains HC! and/or NaOH for pH adjustment, and the insert should be read for precautions and directions before use. The product is distributed by Hospira, Inc. with NDC 0409-3515-11. The lot number and expiration date are also listed however they are not readable by .*
Principal Display Panel (1.5 g Vial Tray)
This is a sterile powder named Flitop Vial containing 1.5g Vancomycin Hydrochloride for intravenous use. It must be diluted before use, and the instructions for the same are given in the insert. The adult dose is 2g daily, diluted with sterile water for injection. The diluted solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. It should be stored prior to reconstitution at 20-25 degrees Celsius and after reconstitution, it can be stored in a refrigerator for 14 days without significant loss of potency. It is distributed by Hospira, Inc. in the USA.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
