Hercessi Injection, Powder, Lyophilized, For Solution
Product Images NDC 69448-015

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 Hercessi (NDC 69448-015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Biopharma 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.

FDA Label Image

Figure 1 (Hercessi 01)

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Figure 2 (Hercessi 02)

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Figure 3 (Hercessi 03)

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Figure 4 (Hercessi 04)

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Figure 5 (Hercessi 05)

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Figure 6 (Hercessi 06)

Figure 6 (Hercessi 06)
This text provides information regarding different treatment regimens for a specific type of disease, including combinations such as doxorubicin + cyclophosphamide, docetaxel + carboplatin + trastuzumab, and more. It also mentions disease-free survival data over a period of years. Additionally, the text includes definitions for the abbreviations AC, T, TCH, and TH. It also refers to Kaplan-Meier estimates being shown.*
FDA Label Image

Figure 7 (Hercessi 07)

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Principal Display Panel (150 mg Vial Carton)

Principal Display Panel (150 mg Vial Carton)
This text provides information about a medication called "HERCESSI" (trastuzumab-strf), an injection with a dosage of 150 mg per vial. It mentions that it is a single-dose vial and instructs to discard any unused solution and not freeze it. The medication is intended for intravenous infusion and should not be shaken after reconstitution. It also advises to store it at 2°C-8°C and protect it from light until the time of reconstitution. The text includes the NDC number for the product and the manufacturer as Accord BioPharma Inc. It gives a directive to reconstitute immediately before use.*
FDA Label Image

Principal Display Panel (150 mg Vial Carton)

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Principal Display Panel (420 mg Vial Carton)

FDA Label Image

Principal Display Panel (420 mg Vial Carton)

Principal Display Panel (420 mg Vial Carton)
This text provides detailed instructions and information about "HERCESSI" (trastuzumab-strf) for injection. The product comes in a 420 mg per vial multiple-dose form and is intended for intravenous infusion after reconstitution. The reconstitution process involves using 20 mL of Bacteriostatic Water for Injection. It is crucial to store the product at 2°C to 8°C until reconstitution, avoid freezing, and protect it from light. The manufacturer is Accord BioPharma Inc., and the product details also include a National Drug Code (NDC) and other technical information. The recommended dosage and additional details can be found in the Prescribing Information.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.