Bortezomib Injection, Powder, Lyophilized, For Solution
Product Images NDC 0409-1703
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Product Visual Gallery
This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Bortezomib (NDC 0409-1703). 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
Figure 1 (Bortezomib 02)
Figure 2 (Bortezomib 03)
Figure 3 (Bortezomib 04)
This is a data table representing the proportion of patients taking Bortezomib and Dexamethasone after different time intervals. The first row indicates the time intervals (in days) and the second row indicates the corresponding number of patients remaining after each time interval. The table also displays a p-value obtained from the log-rank test.*
Figure 4 (Bortezomib 05)
This appears to be a table showing data on patients and the proportion of them who received Bortezomib or Dexamethasone in a study. It includes the number of patients remaining at a certain time point and a p-value from a log-rank test. It is not possible to determine the context or purpose of the study from this limited information.*
Logo (Bortezomib 06)
Principal Display Panel (2.5 mg Vial Label)
This is a description of a pharmaceutical product presented in the form of a lyophilized vial containing 25 mg of bortezomib and 25 mg of mannitol commonly used for injection purposes. The sample also contains cautionary information about the contents of the medication and storage instructions. The recommended dose and additional prescribing documents should also be consulted before utilizing the product.*
Principal Display Panel (2.5 mg Vial Carton)
This is a product information sheet for Bortezomib for Injection, which contains 25 g lyophilized powder along with 25 mg mannitol. The recommended dosage and storage information are provided, and the drug should be reconstituted before use. It can be administered intravenously or subcutaneously, and caution is advised due to the hazardous nature of the drug. The document also includes a lot number and manufacturing information.*
Principal Display Panel (1 mg Vial Label)
Bortezomib for Injection is a hazardous agent that comes in single-dose vial. It is intended for intravenous or subcutaneous use only and must be discarded if the unused portion is left. The manufacturer is Gland Pharma Limited in Andhra Pradesh, India, and it is distributed by Hospira, Inc, Lake Forest, USA. The product code is NDC 0409-1704-01. Unfortunately, no useful information is provided from the alphanumeric code.*
Principal Display Panel (1 mg Vial Carton)
This is a description of Bortezomib medication provided in a single-dose vial containing 1 mg of the drug. It is meant for intravenous or subcutaneous use, and the unused portion should be discarded. The hazardous nature of the drug is indicated by a cautionary label. The medication is supplied in a lyophilized (freeze-dried) form, and the contents of the vial should be reconstituted before use. The recommended dosage and other information on the medication is available in the prescribing information. The drug manufacturer is Hospira, Inc. while the manufacturer of the substance is Gand Phama Limited, located in Andhra Pradesh, India. The label also provides information on how to reconstitute the medicine.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.