Epogen Solution
Product Images NDC 55513-126

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Epogen (NDC 55513-126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amgen, 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

Gather The Other Supplies You Will Need For Your Injection (vial, Syringe, Alcohol Wipes, Cotton Ball, And A Puncture-proof Container For Throwing Away The Syringe And Needle). See Figure 1. (Epogen 03)

An instructional diagram showing components used for medication administration. It includes a vial, a disposable syringe with labeled parts (needle cover, syringe barrel with markings, and plunger rod), alcohol wipes, a cotton ball, and a puncture-proof container with a biohazard symbol.*

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Wash Your Hands Well With Soap And Water Before Preparing The Medicine. See Figure 2. (Epogen 04)

Illustration showing handwashing technique under running water from a faucet, with soap lather and water droplets depicted. The figure emphasizes proper hand hygiene.*

FDA Label Image

Flip Off The Protective Color Cap On The Top Of The Vial. Do Not Remove The Grey Rubber Stopper. Wipe The Top Of The Grey Rubber Stopper With An Alcohol Wipe. See Figures 3 And 4. (Epogen 05)

Two black-and-white illustrations depict hand actions: Figure 3 shows a hand holding a vial, and Figure 4 shows hands opening a vial cap. The images appear to illustrate steps in preparing an injection, likely related to the EPOGEN (epoetin alfa) solution.*

FDA Label Image

Using A Syringe And Needle That Has Been Recommended By Your Healthcare Provider, Carefully Remove The Needle Cover. See Figure 5. Then Draw Air Into The Syringe By Pulling Back On The Plunger. The Amount Of Air Drawn Into The Syringe Should Be Equal To The Amount (ml Or Cc) Of The Epogen Dose Prescribed By Your Healthcare Provider. See Figure 6. (Epogen 06)

An instructional diagram showing two steps for preparing an injection. Figure 5 shows pulling straight off the cap from a vial or syringe. Figure 6 depicts holding a syringe and preparing to inject or withdraw medication. No specific product details are shown in the images.*

FDA Label Image

Push The Plunger Of The Syringe Down To Inject The Air From The Syringe Into The Vial Of Epogen. The Air Injected Into The Vial Will Allow Epogen To Be Easily Withdrawn Into The Syringe. See Figure 7. (Epogen 07)

An instructional line drawing showing hands preparing a syringe by drawing liquid from a vial, likely demonstrating proper extraction technique for the EPOGEN solution. The image features a hand holding a syringe above a vial and an arrow indicating downward movement into the vial.*

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Keep The Needle Inside The Vial. Turn The Vial And Syringe Upside Down. Be Sure The Tip Of The Needle Is In The Epogen Liquid. Keep The Vial Upside Down. Slowly Pull Back On The Plunger To Fill The Syringe With Epogen Liquid To The Number (ml Or Cc) That Matches The Dose Your Healthcare Provider Prescribed. See Figure 8. (Epogen 08)

An instructional illustration showing two hands drawing liquid from a vial into a syringe, labeled as Figure 8. The image likely demonstrates the preparation or administration of the drug Epogen (epoetin alfa) solution for intravenous or subcutaneous use.*

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Keep The Needle In The Vial. Check For Air Bubbles In The Syringe. A Small Amount Of Air Is Harmless. Too Large An Air Bubble Will Give You The Wrong Epogen Dose. To Remove Air Bubbles, Gently Tap The Syringe With Your Fingers Until The Air Bubbles Rise To The Top Of The Syringe. Slowly Push The Plunger Up To Force The Air Bubbles Out Of The Syringe. Keep The Tip Of The Needle In The Epogen Liquid. Pull The Plunger Back To The Number On The Syringe That Matches Your Dose. Check Again For Air Bubbles. If There Are Still Air Bubbles, Repeat The Steps Above To Remove Them. See Figures 9 And 10. (Epogen 09)

An instructional diagram showing hands manipulating a syringe. Figure 9 depicts the plunger being pulled back while holding the needle upright, and Figure 10 shows the plunger being pushed down. The illustrations label the needle and plunger parts of the syringe.*

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Do Not Inject Epogen Into An Area That Is Tender, Red, Bruised, Hard, Or Has Scars Or Stretch Marks. Recommended Sites For Injection Are Shown In Figure 11 Below, Including:○ The Outer Area Of The Upper Arms ○ The Abdomen (except For The 2-inch Area Around The Navel)○ The Front Of The Middle Thighs○ The Upper Outer Area Of The Buttocks (Epogen 0a)

An instructional diagram showing the recommended areas for subcutaneous injection on a human body. The front view highlights the abdomen and thighs, while the back view highlights the upper arms and buttocks as injection sites. This image is consistent with administration instructions for Epogen (epoetin alfa) solution for intravenous or subcutaneous use.*

FDA Label Image

• Clean The Skin With An Alcohol Wipe Where The Injection Is To Be Made. Be Careful Not To Touch The Skin That Has Been Wiped Clean. See Figure 12. (Epogen 0b)

An instructional line drawing illustrating the injection of a substance into the side of a bent knee, depicting proper subcutaneous injection technique likely related to the administration of EPOGEN (epoetin alfa) solution.*

FDA Label Image

• Use The Other Hand To Pinch A Fold Of Skin At The Cleaned Injection Site. Do Not Touch The Cleaned Area Of Skin. See Figure 13. (Epogen 0c)

Illustration labeled Figure 13 showing a hand resting on the front of a bent thigh, likely demonstrating a position or technique related to the use of a medication involving the thigh area.*

FDA Label Image

• Hold The Syringe Like You Would Hold A Pencil. Use A Quick “dart-like” Motion To Insert The Needle Either Straight Up And Down (90-degree Angle) Or At A Slight Angle (45 Degrees) Into The Skin. Inject The Prescribed Dose Subcutaneously As Directed By Your Doctor, Nurse Or Pharmacist. See Figure 14. (Epogen 0d)

An instructional diagram depicting the technique for subcutaneous injection into the thigh. It shows a hand pinching the skin and holding a syringe at either a 45-degree or 90-degree angle relative to the skin surface.*

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• Wipe Off The Venous Port Of The Hemodialysis Tubing With An Alcohol Wipe. See Figure 15. (Epogen 0e)

An instructional illustration labeled Figure 15 showing a hand holding a cloth or wipe and cleaning or preparing a connector or tubing piece. The image depicts part of an intravenous or subcutaneous administration setup, likely related to the preparation of EPOGEN (epoetin alfa) solution for use.*

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Insert The Needle Of The Syringe Into The Cleaned Venous Port And Push The Plunger All The Way Down To Inject All The Epogen. See Figure 16. (Epogen 0f)

An instructional illustration labeled Figure 16 showing a syringe needle inserted into a device or connector attached to tubing. This image likely demonstrates a step in preparing or administering a medication via intravenous or subcutaneous route.*

FDA Label Image

Principal Display Panelndc 55513-126-1010 X 2000 Units/ml Single Dose Vialsamgen®epogen®epoetin Alfarecombinant2000 Units/ml2000 Units/mlsingle Dose Vials (containing 1 mL)for Intravenous Or Subcutaneous Use Onlysterile Solution – No Preservativestore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 11)

Packaging label for EPOGEN (epoetin alfa) recombinant solution, 2000 Units/mL. The label indicates single dose vials with 1 mL sterile solution, free of preservative, for intravenous or subcutaneous use. The product is manufactured by Amgen Inc, Thousand Oaks, CA, with storage instructions to keep between 2° to 8°C (36° to 46°F) and not to freeze or shake. The NDC is 55513-126-10.*

FDA Label Image

Principal Display Panelndc 55513-267-1010 X 3000 Units/ml Single Dose Vialsamgen®epogen®epoetin Alfarecombinant3000 Units/ml3000 Units/mlsingle Dose Vials (containing 1 mL)for Intravenous Or Subcutaneous Use Onlysterile Solution – No Preservativestore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 12)

Packaging label for EPOGEN epoetin alfa recombinant solution, 3000 Units/mL, manufactured by Amgen, Inc. The label indicates 10 single-dose vials of 1 mL each. It states use for intravenous or subcutaneous administration, sterile solution with no preservative, and storage instructions at 2° to 8°C (36° to 46°F), advising not to freeze or shake. Includes Amgen logo, NDC number 55513-267-10, and U.S. License number 1080.*

FDA Label Image

Principal Display Panelndc 55513-148-1010 X 4000 Units/ml Single Dose Vialsamgen®epogen®epoetin Alfarecombinant4000 Units/ml4000 Units/mlsingle Dose Vials (containing 1 mL)for Intravenous Or Subcutaneous Use Onlysterile Solution – No Preservativestore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 13)

Packaging label for EPOGEN epoetin alfa 4000 Units/mL solution. The label states it is a sterile, preservative-free single dose vial containing 1 mL for intravenous or subcutaneous use. Manufactured by Amgen Inc. The label includes storage instructions and the NDC 55513-148-10. The design features the Amgen logo and product information in red, green, and black text on a white background.*

FDA Label Image

Principal Display Panelndc 55513-144-1010 X 10,000 Units/ml Single Dose Vialsamgen®epogen®epoetin Alfarecombinant10,000 Units/ml10,000 Units/mlsingle Dose Vials (containing 1 mL)for Intravenous Or Subcutaneous Use Onlysterile Solution – No Preservativestore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 14)

Packaging label for EPOGEN epoetin alfa solution, 10,000 Units/mL, in single dose vials. The label specifies recombinant epoetin alfa, marketed by Amgen Inc. It includes dosing form instructions for intravenous or subcutaneous use, sterile solution without preservative, and storage conditions between 2° to 8°C (36° to 46°F). The label displays NDC 55513-144-10 and highlights it is for prescription use only.*

FDA Label Image

Principal Display Panelndc 55513-283-10amgen®epogen®epoetin Alfarecombinantmultiple Dose Vials20,000 Units/2 mL (10,000 Units/ml)20,000 Units/2 mL (10,000 Units/ml)for Intravenous Or Subcutaneous Use Onlysterile Solution – Preserved2 mLstore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 15)

Packaging label for Epogen epoetin alfa recombinant solution, 20,000 Units/2 mL (10,000 Units/mL) in a 2 mL multiple dose vial. The label states the medication is for intravenous or subcutaneous use only, is sterile and preserved. It includes storage instructions (2° to 8°C), and the labeler Amgen Inc with U.S. licensing information.*

FDA Label Image

Principal Display Panelndc 55513-478-10amgen®epogen®epoetin Alfarecombinantmultiple Dose Vials20,000 Units/ml20,000 Units/ml1 mLfor Intravenous Or Subcutaneous Use Onlysterile Solution – Preservedstore At 2˚ To 8˚c (36˚ To 46˚f). Do Not Freeze Or Shake.manufactured By Amgen Inc.thousand Oaks, Ca 91320-1799 U.s.a.u.s. License No. 1080©2012,2017 Amgen Inc.rx Only (Epogen 16)

The packaging label for Epogen epoetin alfa 20,000 units/mL solution in a 1 mL multiple-dose vial. The label states it is for intravenous or subcutaneous use only, preserved sterile solution, manufactured by Amgen Inc. Storage instructions specify 2° to 8°C (36° to 46°F) and advise against freezing or shaking.*

* 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.