Alymsys Injection, Solution
Product Images NDC 70121-1755

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Alymsys (NDC 70121-1755). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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.

FDA Label Image

Figure 1 (Alymsys Bevacizumab Maly Injection 1)

Figure 1 (Alymsys Bevacizumab Maly Injection 1)
This appears to be a clinical trial progress chart showing the number of patients and time in months. Two different treatment groups (IFL + Placebo and IFL + Bevacizumab) are being compared. However, without more context or information, it is not possible to draw any further conclusions from this text.*
FDA Label Image

400mg Carton (Alymsys Bevacizumab Maly Injection 10)

400mg Carton (Alymsys Bevacizumab Maly Injection 10)
This is a description of Alymsys, a medication manufactured by Amneal Pharmaceuticals LLC in Bridgewater, NJ, USA. The medication is produced in Spain with a US License number 2241. It comes in a single-dose vial with a preservative-free 400 mg/16 mL dose (25mg/mL) for Intravenous Infusion after dilution. The diluted medication must be administered only for the prescribed use. The product should be refrigerated at 2°C to 8°C (36°F to 46°F) and stored in the original carton. It is essential to avoid freezing or shaking. The package contains instructions, including dosage directives.*
FDA Label Image

Figure 2 (Alymsys Bevacizumab Maly Injection 2)

FDA Label Image

Figure 3 (Alymsys Bevacizumab Maly Injection 3)

FDA Label Image

Figure 4 (Alymsys Bevacizumab Maly Injection 4)

FDA Label Image

Figure 5 (Alymsys Bevacizumab Maly Injection 5)

FDA Label Image

Figure 6 (Alymsys Bevacizumab Maly Injection 6)

FDA Label Image

100 mg Label (Alymsys Bevacizumab Maly Injection 7)

100 mg Label (Alymsys Bevacizumab Maly Injection 7)
This is a description of a medication called Alymsys with the active ingredient bevacizumab given through injection or intravenous infusion. It comes in a single-dose vial of 1100 mg/4 mL (25 mg/mL) and must be stored refrigerated between 2-8°C (36°F to 46°F) in the original carton to protect it from light. It cannot be frozen or shaken and contains no preservatives. Dilution in 0.9% Sodium Chloride Injection, USP is necessary before intravenous use. Dosage instructions can be found in the prescribing information. The medication is manufactured by Amneal Pharmaceuticals and the product is a property of SPAN.*
FDA Label Image

100mg Carton (Alymsys Bevacizumab Maly Injection 8)

100mg Carton (Alymsys Bevacizumab Maly Injection 8)
This is a description of an injectable medication packaging by Amneal Pharmaceuticals called Alymsys. It is manufactured in Spain and has a concentration of 1100 mg/4 mL (25 mg/mL). The medication comes in a single-dose vial that should be stored in the original carton in refrigeration between 2°C to 8°C (36°F to 46°F). It should not be frozen or shaken, contains no preservatives, and must be diluted with 0.9% Sodium phloride Injection, USP before Intravenous Infusion. The preservative-free 100 mg/4 mL (25 mg/mL) single-dose vial of ALYMSYS is composed of 25 mg bevacizumab, 60 mg a, a-trehalose dihydrate, 0.4 mg polysorbate 20, 1.2 mg sodium phosphate (dibasic, anhydrous), 5.8 mg sodium phosphate (monobasic, monohydrate), and water for injection, USP. Dosage should be determined by a licensed medical practitioner according to the prescribing information.*
FDA Label Image

400mg Label (Alymsys Bevacizumab Maly Injection 9)

400mg Label (Alymsys Bevacizumab Maly Injection 9)
This is a description of a medicine called evacizumab-ma y. The medicine must be stored in a cool and protected place, but should not be frozen or shaken. The dosage information is available with the prescribing information. The medicine should be diluted in 0.9% Esic! for intravenous infusion, and the unused portion should be discarded.*

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