Carton Label-1.25 (Carton Label 1.25g)
Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 82449-005
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 82449-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Steriscience Specialties Private Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Carton Label 1.5g (Carton Label 1.5g)
Carton-label-750 (Carton Label 750 mg)
Structure (Vanco)
Vial-1-25g (Vial Label 1.25 Gram)
This is a description of Vancomycin Hydrochloride for Injection, USP. It is a sterile powder in a single-dose vial with a concentration of 1.25 g/vial. The medication is for intravenous use and must be reconstituted and diluted before administration. The text emphasizes the importance of reading the package insert for precautions and directions before use. The usual adult dosage is provided in the package insert. The reconstituted solution should be stored at 20° to 25°C (68°F to 77°F) or in the refrigerator for up to 14 days. The medication is manufactured by Steierscience in Warsaw, Poland.*
Vial-1-5g (Vial Label 1.5 Gram)
This is a label for Vancomycin Hydrochloride for Injection, USP. It contains 1.5 g of Vancomycin per vial and is for intravenous use. The medication must be further diluted after reconstitution. The package insert should be read for precautions and directions before use. The usual adult dosage can be found in the package insert as well. The product can be stored between 68-77°F (20-25°C) before reconstitution. Once reconstituted, it can be stored in a refrigerator for up to 14 days without significant loss of potency. The manufacturer is listed as Seiscience Sp. z o.o. with an address in Poland.*
Vial-label-750 (Vial Label 750 mg)
This is a prescription medicine with the NDC code 82449-005-01 for Vancomycin Hydrochloride for Injection, USP. It is intended for intravenous use and must be diluted after reconstitution according to the package insert. Each single-dose vial contains 750 mg of vancomycin. The manufacturer is Steris Corporation and the address is 20.0. Lot NO VARNISH ZONE. The expiration date is overcoded. Users should refer to the package insert for precautions and directions.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
