Prolastin-c Liquid Injection, Solution
Product Images NDC 13533-705

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

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prolastin-c Liquid (NDC 13533-705). 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

3061390 Carton

3061390 Carton
Box label for Prolastin-C Liquid 1000 mg/20 mL injection, containing Alpha1-Proteinase Inhibitor (Human). The label indicates it is a plasma derivative solution for intravenous use, manufactured by Grifols USA, LLC. The label includes dosage form, storage instructions, and warnings, with a barcode and NDC 13533-705.*
FDA Label Image

Figure 1 (Figure1)

Figure 1 (Figure1)
A line graph comparing Alpha1-Proteinase Inhibitor (Alpha1-PI) concentration (mg/mL) over nominal time (hours) between Prolastin-C Liquid and Prolastin-C. The graph shows concentration declining from about 2.0 mg/mL at time zero to approximately 0.6 mg/mL at 168 hours, with values for both products closely overlapping throughout the time course.*
FDA Label Image

Prolastin-c Liquid Vial (Label)

Prolastin-c Liquid Vial (Label)
Label for Prolastin-C Liquid 1000 mg/20 mL injection solution, containing Alpha1-Proteinase Inhibitor (Human). The label states it is solvent detergent treated and nanofiltered for intravenous use only. It includes storage instructions to keep at 2 to 8°C and warnings against freezing or using after expiration. The product is labeled by Grifols Therapeutics LLC, Research Triangle Park, NC.*

* 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.