Gamastan Injection, Solution
Product Images NDC 13533-635

4 FDA label images from Grifols Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Gamastan (NDC 13533-635). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grifols Usa, Llc, 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

FDA Label Image

10milvial

10milvial
Label for GAMASTAN Immune Globulin (Human) injection solution, 10 mL vial, by Grifols Therapeutics LLC. The label includes warnings about administration and dosage instructions, specifies it as a plasma derivative for intramuscular use, and provides manufacturer and licensing information.*
FDA Label Image

Carton

Carton
Label for GAMASTAN Immune Globulin (Human) Injection, Solution 0.165 g/mL, a plasma derivative for intramuscular use. The label indicates a 10 mL single-dose vial, produced by Grifols USA, LLC. The label includes storage instructions, warnings against intravenous use, and manufacturing details.*
FDA Label Image

Grifols

Grifols
FDA Label Image

Rabiesvirusantibodylevels

Rabiesvirusantibodylevels
A line graph depicting mean (standard deviation) rabies virus antibody levels (IU/mL) over time following a single 20 IU/kg dose of HYPERRAB (300 IU/mL) administered by intramuscular injection. The x-axis represents time in hours, ranging from 0 to 504 hours, and the y-axis shows antibody levels from 0 to 0.2 IU/mL. Data points with error bars illustrate antibody levels rising rapidly within the first 48 hours and then plateauing up to 504 hours.*

* 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.