Panzyga Solution
Product Images NDC 0069-1109

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Panzyga (NDC 0069-1109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer 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

Image File (Img0001)

A data table titled 'Virus Reduction Factor log10' showing comparison of virus reduction factors for enveloped viruses (HIV-1, PRV, BVDV) and non-enveloped viruses (MEV, PPV) across different production steps: S/D treatment, ion-exchange chromatography, nanofiltration (20 nm), and global reduction factor. Values include numeric reduction factors and some entries marked 'n.d.' indicating not detected.*

FDA Label Image

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A table presenting pharmacokinetic parameters for Panzyga (immune globulin intravenous human) across different age groups (0-<6, 6-<12, 12-<16, 16-75 years). It compares baseline uncorrected and corrected values for Cmax, AUC, clearance (CL), volume of distribution (Vss), and half-life with means and standard deviations.*

FDA Label Image

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A data table presenting pharmacokinetic parameters including Cmax, AUC, clearance (CL), volume of distribution (Vss), and half-life across different age groups (0-<6 years, 6-<12 years, 12-<16 years, and 16-75 years). The table compares baseline uncorrected and baseline corrected values, providing means and standard deviations for each parameter.*

FDA Label Image

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Packaging label for Panzyga 1 g/10 mL solution, an intravenous immune globulin (human) 10% product. The label includes storage instructions, manufacturing details by Pfizer Laboratories, and indicates the solution is solvent/detergent treated and nanofiltered. The label displays the NDC 0069-1011-02 and states the product is for intravenous infusion only.*

FDA Label Image

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Packaging label for Panzyga immune globulin intravenous (human) 10% solution, 2.5 g per 25 mL vial. The label indicates the product is solvent/detergent treated and nanofiltered for intravenous infusion use only. Manufactured by Pfizer Laboratories Div Pfizer Inc and includes storage instructions and regulatory information.*

FDA Label Image

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The packaging label for Panzyga 5 g/50 mL intravenous immune globulin solution shows branding by Pfizer Laboratories Div Pfizer Inc. It includes storage instructions, manufacturer details in Austria, and specifies the product as solvent/detergent treated and nanofiltered. The label states the product is for intravenous infusion only and is for prescription use.*

FDA Label Image

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Panzyga 10 g/100 mL solution carton label for immune globulin intravenous (human) 10%, a plasma derivative by Pfizer Laboratories Div Pfizer Inc. The packaging displays storage instructions, manufacturing details marked as 'Made in France', and usage notes including solvent/detergent treated and nanofiltered attributes.*

FDA Label Image

Image File (Img0008)

Packaging label for Panzyga immune globulin intravenous (human) solution, 100 mg/mL strength. The label indicates a 20 g, 200 mL vial and states the product is solvent/detergent treated and nanofiltered, for intravenous infusion only. Manufactured by Pfizer Laboratories, the label includes storage instructions, barcodes, and dosage information.*

FDA Label Image

Image File (Img0009)

Label for Panzyga immune globulin intravenous (human) solution, 30 g in 300 mL (100 mg/mL). The label indicates it is solvent/detergent treated and nanofiltered for intravenous infusion only. Manufactured by Octapharma and distributed by Pfizer Labs. Storage instructions and dosage information are included, along with regulatory and barcode details.*

* 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.