Arixtra Injection, Solution
Product Images NDC 67457-593

26 FDA label images from Mylan Institutional Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 26 technical images submitted to the FDA as part of the official labeling for Arixtra (NDC 67457-593). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

2.7 Figure A (Image 05)

2.7  Figure A (Image 05)
An illustration of a syringe labeled with annotations. It shows the syringe plunger (2), barrel (3), and needle (4), representing a device used for administering injection solutions.*
FDA Label Image

2.7 Figure B (Image 06)

2.7 Figure B (Image 06)
An instructional illustration showing a syringe labeled with numbers 2, 3, and 4, likely demonstrating steps or parts related to the preparation or administration of an injection. The syringe appears to have a cap or needle cover on the right side.*
FDA Label Image

2.7 Figure C (Image 07)

2.7 Figure C (Image 07)
An instructional illustration showing a person preparing to administer a subcutaneous injection. The individual is seated on a cushioned surface with one leg bent and the other extended, holding the injection device near the abdomen area, demonstrating proper technique for subcutaneous injection.*
FDA Label Image

Fondaparinux Sodium Structural Formula (Image 08)

Fondaparinux Sodium Structural Formula (Image 08)
A black and white illustration showing a hand holding a capped syringe and another hand removing the cap with a twisting motion, indicated by arrows. This instructional diagram likely demonstrates how to prepare the syringe for injection.*
FDA Label Image

Arixtra Prefilled Syringe (Image 09)

Arixtra Prefilled Syringe (Image 09)
Black and white instructional illustration showing a person pressing their side abdomen with both hands. Two arrows point to the area being pressed, possibly indicating an injection site or a location relevant to the medication Arixtra (fondaparinux sodium) subcutaneous injection.*
FDA Label Image

Ifu Parts Of Arixtra Syringe (Image 10)

Ifu Parts Of Arixtra Syringe (Image 10)
An instructional illustration showing a person administering a subcutaneous injection into the abdominal area using a syringe. The individual pinches the skin to prepare for the injection, consistent with common subcutaneous injection techniques.*
FDA Label Image

Ifu Syringe Before Use (Image 11)

Ifu Syringe Before Use (Image 11)
An instructional black and white illustration showing a hand holding a syringe with a label marked 'Arixtra 7.5 mg' (fondaparinux sodium injection, solution) and an arrow pointing to the label area, demonstrating preparation or identification of the product for subcutaneous administration.*
FDA Label Image

Ifu Syringe After Use (Image 12)

Ifu Syringe After Use (Image 12)
An instructional illustration displaying a hand holding a syringe for subcutaneous injection. An arrow indicates the direction or action in the injection procedure, emphasizing how to properly administer the injection.*
FDA Label Image

Ifu Figure A (Image 13)

Ifu Figure A (Image 13)
Packaging label for Arixtra (fondaparinux sodium injection, USP) 2.5 mg/0.5 mL, a subcutaneous injection by Mylan Institutional LLC. The label states it contains 10 single-dose, prefilled syringes with an automatic needle protection system and includes instructions for pharmacists to dispense the patient information leaflet.*
FDA Label Image

Ifu Figure B (Image 14)

Ifu Figure B (Image 14)
Packaging label for Arixtra 5 mg/0.4 mL injection, solution containing fondaparinux sodium for subcutaneous use. The label indicates it is a prescription drug by Mylan Institutional LLC. The box contains 10 single-dose, prefilled syringes equipped with an automatic needle protection system. The label includes directions for pharmacists to dispense a patient information leaflet with each package.*
FDA Label Image

Ifu Figure C (Image 15)

Ifu Figure C (Image 15)
Arixtra 7.5 mg/0.6 mL (fondaparinux sodium injection, USP) carton for subcutaneous injection. The label indicates it contains 10 single-dose prefilled syringes with an automatic needle protection system. Labeler is Mylan Institutional LLC. The packaging includes dosing information and storage instructions, highlighting Rx only status.*
FDA Label Image

Ifu Figure D (Image 16)

Ifu Figure D (Image 16)
Arixtra 10 mg/0.8 mL injection solution label for subcutaneous use. The packaging states the generic name fondaparinux sodium injection, USP, and indicates it contains 10 single-dose prefilled syringes with an automatic needle protection system. The label is from Mylan Institutional LLC and includes instructions for pharmacists to dispense an accompanying patient information leaflet.*
FDA Label Image

Ifu Figure E (Image 17)

Ifu Figure E (Image 17)
An instructional illustration showing a hand holding a prefilled syringe of Arixtra (fondaparinux sodium) injecting subcutaneously into the skin. An arrow indicates the injection step for subcutaneous administration.*
FDA Label Image

Ifu Figure F (Image 18)

Ifu Figure F (Image 18)
An instructional illustration showing a hand pulling back the plunger of a syringe, with an arrow indicating the direction of pull. The syringe contains a liquid and is positioned near a finger, suggesting preparation for subcutaneous injection.*
FDA Label Image

Ifu 2 Pharmacy Prepared Syringe (Image 19)

Ifu 2 Pharmacy Prepared Syringe (Image 19)
A black and white line drawing of a syringe with a needle attached, featuring volume markings on the barrel from 0.1 to 1.0 mL. The syringe is depicted horizontally with the plunger on the right side.*
FDA Label Image

Ifu 2 Parts Of The Arixtra Syringe (Image 20)

Ifu 2 Parts Of The Arixtra Syringe (Image 20)
Line drawing illustration of a syringe labeled with numbers 1, 2, and 3 pointing to the needle, barrel with measurement markings, and plunger, respectively. The syringe is shown for subcutaneous injection use, consistent with Arixtra (fondaparinux sodium) injection administration.*
FDA Label Image

Ifu 2 Figure A (Image 21)

Ifu 2 Figure A (Image 21)
An illustration showing the lower stomach area (abdomen) on a front view of a human torso, highlighting the recommended site for subcutaneous injection.*
FDA Label Image

Ifu 2 Figure B (Image 22)

Ifu 2 Figure B (Image 22)
An instructional black and white line drawing showing one hand holding a syringe and the other hand pulling on the plunger to withdraw fluid. The illustration includes a directional arrow indicating the movement of the plunger during injection preparation.*
FDA Label Image

Ifu 2 Figure C (Image 23)

Ifu 2 Figure C (Image 23)
An instructional illustration showing a hand pressing on the skin to form a fold or pinch, typically used to demonstrate the proper technique for subcutaneous injection administration.*
FDA Label Image

Ifu 2 Figure D (Image 24)

Ifu 2 Figure D (Image 24)
Instructional illustration showing a hand holding a syringe positioned at a 90-degree angle to the skin, indicating subcutaneous injection technique for administering medication, with a downward arrow emphasizing needle insertion direction.*
FDA Label Image

Ifu 2 Figure E (Image 25)

Ifu 2 Figure E (Image 25)
An instructional illustration showing a hand administering a subcutaneous injection using a syringe inserted at a downward angle into the skin, demonstrating the proper technique for subcutaneous injection delivery.*
FDA Label Image

Ifu 2 Figure F (Image 26)

Ifu 2 Figure F (Image 26)
Illustration showing the administration of a subcutaneous injection using a syringe. A hand holds the syringe inserted into the skin, while the other hand pulls the plunger upward, indicating the process of drawing medication or injection technique.*
FDA Label Image

Arixtra Injection 2.5 mg/0.5 mL Carton Label (Image 01)

Arixtra Injection 2.5 mg/0.5 mL Carton Label (Image 01)
Instructional illustrations showing correct use of a prefilled syringe for Arixtra (fondaparinux sodium) injection. Figure 1 demonstrates removing the cap from the syringe needle, and Figure 2 shows administration of the subcutaneous injection into the abdominal area.*
FDA Label Image

Arixtra Injection 5 mg/0.4 mL Carton Label (Image 02)

Arixtra Injection 5 mg/0.4 mL Carton Label (Image 02)
Two black and white instructional images showing subcutaneous injection technique. The first image (Figure 3) depicts a person preparing to inject a syringe into an area of the abdomen. The second image (Figure 4) shows the syringe inserted into the skin, with an arrow indicating the injection process. These illustrations likely demonstrate how to administer a subcutaneous injection.*
FDA Label Image

Arixtra Injection 7.5 mg/0.6 mL Carton Label (Image 03)

Arixtra Injection 7.5 mg/0.6 mL Carton Label (Image 03)
Chemical structure of fondaparinux sodium, the active ingredient in Arixtra injection solution. The diagram shows the molecular arrangement with sodium (Na) ions and functional groups characteristic of fondaparinux.*
FDA Label Image

Arixtra Injection 10 mg/0.8 mL Carton Label (Image 04)

Arixtra Injection 10 mg/0.8 mL Carton Label (Image 04)
An instructional diagram of a syringe assembly for subcutaneous injection. The image shows numbered components including a needle cap, plunger, syringe barrel, and vial connector, illustrating parts involved in preparing and administering an injection.*

* 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.