Vancomycin Hydrochloride Structural Formula (Image 01)
Vancomycin Hydrochloride Injection, Solution
Product Images NDC 0338-3583
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 31 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0338-3583). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Baxter Healthcare Corporation, 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
Vancomycin Representative Container Label Ndc 0338-3551-48 (Image 02)
This is a description of Vancomycin Injection in 5% Dextrose. It is a single-dose container that is sterile and contains 500 mg of vancomycin in 100 mL with approximately 5 g of Dextrose Hydrous. Its recommended dosage is for intravenous use only, and caution must be taken not to add supplementary medication or additives. Thawing should be done at room temperature or under refrigeration, and thawed solution is stable for 30 days under refrigeration or 72 hours at room temperature. This product should not be refrozen.*
Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 1 Of 3 (Image 03)
This text provides instructions for thawing and handling a product stored in a PL 2040 plastic container. The product should be thawed at room temperature or in refrigeration, and should not be thawed through immersion in water or microwave radiation. Thawed solution remains chemically stable for 72 hours at room temperature or for 30 days under refrigeration. The text also warns against forcing a thaw or refreezing the product, and advises handling frozen product containers with care.*
Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 2 Of 3 (Image 04)
Vancomycin Injection, USP in 5% Dexirose is a medication for intravenous use only. Each bag comes with 500 mg per 100 mL (5 mg/mL) in a total of 6 single-use bags. It is iso-osmolic and should be stored at or below -20°C/4°F. The National Drug Code (NDC) is 0338-3551-48 and the corresponding code is 2G3551. The text also includes a bar code for product identification.*
Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 3 Of 3 (Image 05)
This is a description for GALAXY Container Sterile Nonpyrogenic, a solution for intravenous use. Each 100 mL of the solution contains Vancomycin Hydrochloride 500 mg and approximately 5 g of Dextrose Hydrous in water for injection. The solution's pH may have been adjusted with hydrochloric acid and/or sodium hydroxide. It is cautioned not to add supplementary medication or additives to the solution. Baxter and Galaxy are registered trademarks of Baxter International Inc.*
Vancomycin Representative Container Label 0338-3552-48 (Image 06)
Vancomycin Representative Carton Label 0338-3552-48 Panel 1 Of 3 (Image 07)
Vancomycin Injection, USP with 5% Dextrose, GALAXY Code 263552 is a single-dose, sterile, nonpyrogenic container available in 5 mg/mL strength. It is intended for intravenous use only and should not be mixed with other medications or additives. Each 100 mL of the solution contains Vancomycin Hydrochloride, USP equivalent to 500 mg vancomycin with Dextrose Hydrous, USP in Water for Injection, USP. The pH level may be adjusted with hydrochloric acid and/or sodium hydroxide. The product should be stored at or below -20°C (-4°F) and should not be thawed by immersion in water baths or by microwave. Baxter and Galaxy are registered trademarks of Baxter International Inc.*
Vancomycin Representative Carton Label 0338-3552-48 Panel 2 Of 3 (Image 08)
This is a set of instructions regarding the thawing and handling of a frozen product contained in PL 2040 plastic containers. The product can be thawed at room temperature or under refrigeration, but not by immersion in water baths or microwave irradiation. The thawed solution remains chemically stable for a limited time at room temperature and refrigeration. The containers should be handled with care as they may be fragile in the frozen state.*
Vancomycin Representative Carton Label 0338-3552-48 Panel 3 Of 3 (Image 09)
Vancomycin Injection, USP in 5% dextrose solution is only available through prescription. The product has a code of 2G3552 and comes in a package of 3 single-use bags, with each bag containing 200 liters of isotonic solution. The product must be stored below -20°C/4°F. The barcode for this product is (01) 20303383552482.*
Vancomycin Representative Container Label 0338-3580-48 (Image 10)
This is a description of the GALAXY Container Sterile, a nonpyrogenic solution meant for intravenous use only. Each 100 ml contains Vancomycin Hydrochloride, USP equivalent to either 500 or 800 mg vancomycin, depending on the version. The solution also has Dextrose Hydrous, USP in Water for Injection, USP, and the pH may have been adjusted with hydrochloric acid and/or sodium hydroxide. It is cautioned that no supplementary medication or additives should be added to this solution. The trademarks Baxter and Galaxy are registered by Baxter International Inc.*
Vancomycin Representative Carton Label 0338-3580-48 Panel 1 Of 3 (Image 11)
Vancomycin Representative Carton Label 0338-3580-48 Panel 2 Of 3 (Image 12)
This is a description of a medication called Vancomycin Injection, USP, which is administered intravenously, and must not have supplementary medication or additives added to it. The medication comes in a single-dose container that is sterile and non-pyrogenic, and the unused portion must be discarded. This medication is stored at or below -20°C (-4°F) and should not be thawed by immersion in water baths or by microwave irradiation. Thawed solution is stable for 30 days under refrigeration or 72 hours at room temperature. The medication is made up of 750mg of Vancomycin and 5% dextrose in a 150mL solution.*
Vancomycin Representative Carton Label 0338-3580-48 Panel 3 Of 3 (Image 13)
This text provides instructions for handling and thawing a product stored in a plastic container with the code PL 2040. It advises to thaw the product either at room temperature or under refrigeration and warns against immersing it in water or using microwave radiation. The thawed solution remains chemically stable for a limited time and should not be refrozen. The text cautions that frozen product containers may be fragile and need to be handled with care.*
Vancomycin Representative Container Label 0338-3581-01 (Image 14)
This is a description of Vancomycin Injection, USP in 5% dextrose, which is only available by prescription. It comes in a package of 3 single-use bags, each containing 150mL. The product is Iso-osmolic, and it should be stored at or below -20°C/-4°F. The NDC code for this injection is 0338-3580-48, while the code for the package is 2G3580. There are two barcodes shown, one with the code and the other for the bar code position, which is for reference only.*
Vancomycin Representative Carton Label 0338-3581-01 Panel 1 Of 3 (Image 15)
This is a description of GALAXY Container Sterile Nonpyrogenic, a solution for intravenous use only. It contains Vancomycin Hydrochloride, with a 500 mg equivalent of vancomycin and 5 g Dextrose Hydrous in water for injection. The pH may have been adjusted. It is cautioned not to add other medications or additives. Baxter and Galaxy are registered trademarks of Baxter International Inc. The recommended dosage is found in the prescribing information.*
Vancomycin Representative Carton Label 0338-3581-01 Panel 2 Of 3 (Image 16)
Vancomycin Representative Carton Label 0338-3581-01 Panel 3 Of 3 (Image 17)
NDC 0338-3581-01 is a vancomycin injection contained in a single-dose container. Each container contains 500mg/100 mL of Vancomycin Hydrochloride in 0.9% Sodium Chloride. It is sterile and nonpyrogenic, and should not be used with other medications. It is intended for intravenous use only, and should be thawed at room temperature or under refrigeration. Thawed solution is stable for 30 days under refrigeration or 72 hours at room temperature. The product should not be refrozen.*
Vancomycin Representative Container Label 0338-3582-01 (Image 18)
This text provides instructions for thawing and handling a product stored in a plastic container labeled PL 2040. The product should be thawed either at room temperature or under refrigeration and should not be thawed by immersion in water baths or microwaving, nor should it be force-thawed. Once thawed, the solution in the container remains chemically stable for 72 hours at room temperature or 30 days when refrigerated. The container should not be refrozen, and should be handled with care as it may be fragile in the frozen state.*
Vancomycin Representative Carton Label 0338-3582-01 Panel 1 Of 3 (Image 19)
Vancomycin Injection, USP in 0.9% Sodium Chloride is a prescription medicine that comes in six single-dose bags, each containing 500 mg of vancomycin in 100 mL of solution. Each bag is stored at or below -20°C/-4°F and is iso-osmotic. The product is identified by the NDC code 0338-3581-01 and the barcode (01) 20303383581017, for scanning purposes only.*
Vancomycin Representative Carton Label 0338-3582-01 Panel 2 Of 3 (Image 20)
The GALAXY Container is a sterile, nonpyrogenic solution that contains 500 mg Vancomycin Hydrochloride USP and approximately 0.9 g Sodium Chloride USP per 100 mL of Water for Injection USP. The pH of the solution may have been adjusted with hydrochloric acid and/or sodium hydroxide. This solution is for intravenous use only and caution should be taken not to add any supplementary medications or additives. Baxter and Galaxy are registered trademarks of Baxter International Inc, operated by Baxter Healthcare Corporation located in Deerfield, Illinois, USA.*
Vancomycin Representative Carton Label 0338-3582-01 Panel 3 Of 3 (Image 21)
Vancomycin Representative Container Label 0338-3583-01 (Image 22)
This is a description of the Vancomycin Injection, USP. It comes in a single-dose container and is sterile non-pyrogenic. Each 150 mL container has 750 mg of Vancomycin Hydrochloride, USP with approximately 0.9 Sodium Chloride, USP in Water for Injection, USP. It is meant for intravenous use only as per prescribing information. The solution should not be thawed by immersion in water baths or microwave irradiation. The thawed solution is stable for 30 days under refrigeration or 72 hours at room temperature. It should not be refrozen. The product should be stored at or below -20°C (-4°F) and thawed at room temperature (25°C/77°F) or under refrigeration (5°C/41°F). Any unused portion should be discarded.*
Vancomycin Representative Carton Label 0338-3583-01 Panel 1 Of 3 (Image 23)
The text describes instructions for thawing and handling of a product stored in GA plastic container (PL 2040). Thawing should be done at room temperature or under refrigeration and should not be done by immersion in water baths or microwave. The thawed solution remains chemically stable for 72 hours at room temperature or for 30 days when refrigerated. Refreezing is not recommended. The text also mentions that frozen product containers should be handled with care as they may be fragile.*
Vancomycin Representative Carton Label 0338-3583-01 Panel 2 Of 3 (Image 24)
Vancomycin Injection is a medicine available with a prescription in Rx only form. It is presented in 3 bags of 150 mL each of 750 mg per 150 mL (5 mg/mL) of Vancomycin Injection USP dissolved in 0.9% sodium chloride. The solution must be stored at or below -20°C-4°F. Each bag is isosmotic. The barcode is only for position purposes.*
Vancomycin Representative Carton Label 0338-3583-01 Panel 3 Of 3 (Image 25)
This is a description of GALAXY Container, which is sterile and non-pyrogenic. It includes Vancomycin Hydrochloride, USP equivalent to 500mg Vancomycin with approximately 0.8g Sodium Chloride, USP in Water for Injection, USP. The pH can be adjusted with hydrochloric acid and/or sodium hydroxide. This container is for intravenous use only and the recommended dosage needs to be taken according to the prescribing information. It is cautioned not to add supplementary medication or additives. Baxtor and Galaxy are registered trademark of Baxter International Inc. The manufacturer is Baxter Healthcare Corporation located in Deerfield, Illinois, USA.*
Image 26
Image 27
Vancomycin Injection is a sterile solution containing 1g of Vancomycin per 200 mL in 0.9% Sodium Chloride, for intravenous use only. Each 100 mL contains Vancomycin Hydrochloride equivalent to 13 500 mg Vancomycin in 0.9 Sodium Chloride, USP, in Water for Injection. The solution can only be thawed at room temperature or under refrigeration, and the thawed solution is stable for 30 days under refrigeration or 72 hours at room temperature. Adding supplementary medication or additives is not recommended. *
Image 28
This text provides instructions for properly thawing a specific product stored in a plastic container (PL 2040) at room temperature or in refrigeration. It advises against using water baths or microwaving to thaw and warns against forcing the thaw. The thawed solution is chemically stable for a limited time at room temperature or refrigeration, and it should not be refrozen. Additionally, the text warns that the product containers may be fragile in the frozen state and recommends handling with care.*
Image 29
Vancomycin Injection, USP in 0.9% sodium chloride is a medication available only by prescription. Each bag contains 1g per 200mL and there are three single-dose bags. The solution is iso-osmotic and should be stored at or below -20°C/-4°F. The barcode should be positioned correctly for scanning.*
Image 30
This is a description of GALAXY Container Sterile Nonpyrogenic, which is a medication that contains Vancomycin Hydrochloride, USP equivalent to 500 mg and approx. 0.8 g Sodium Chioride, USP in Water for Injection, USP. The pH level may be adjusted with hydrochloric acid and/or sodium hydroxide. It is for intravenous use only and additional medications or additives should not be added. Baxter and Galaxy are registered trademarks of Baxter International Inc.*
Image 31
* 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.
