safe sharps disposal, and for specific information about sharps disposal in the state that you live in, go to FDA’s website at: http://www.fda.gov/safesharpsdisposal.
Keep children away from the used On-body Injector.
If the status light is flashing red, you may not have received your full dose. Call your healthcare provider immediately.
If the adhesive becomes saturated with fluid, or you see dripping, your medicine may have leaked out.
Even with a leak, the status light may remain green and the fill indicator may be at EMPTY.
Call your healthcare provider immediately as you may not have received your full dose.
Note: It is normal to see a few drops of fluid at the application site, but not normal to see a noticeably wet (saturated) adhesive.
Call your healthcare provider immediately if the On-body Injector at any time comes away from your skin before your full dose delivery, DO NOT reapply it.
If there is blood, press a clean cotton ball or gauze pad on the application site. Apply an adhesive bandage if needed.
Call your healthcare provider immediately if you experience persistent or worsening redness or tenderness at the application site, as this can be a sign of infection.
Neulasta® (pegfilgrastim)
Manufactured by:
Amgen Inc.
One Amgen Center Drive
Thousand Oaks, California 91320-1799
US License No. 1080
Patent: http://pat.amgen.com/neulasta/
© 2002 to 2015 Amgen Inc. All rights reserved.
www.neulasta.com
1-844-MYNEULASTA (1-844-696-3852) Issued: 11/2015 v4
PRINCIPAL DISPLAY PANEL
Principal Display Panel
NDC 55513-190-01
1 - 0.6 mL Single Use Prefilled Syringe
AMGEN®
Neulasta ®
(pegfilgrastim)
Pegylated Recombinant Methionyl Human Granulocyte Colony-Stimulating Factor
(PEG-r-metHuG-CSF) derived from E Coli
6 mg
6 mg in 0.6 mL Single Use Prefilled Syringe
For Subcutaneous Use Only
This Product Contains Dry Natural Rubber
Sterile Solution – No Preservative
Rx Only
Manufactured by Amgen Inc.
Thousand Oaks, CA 91320-1799 U.S.A.
U.S. License No. 1080
PRINCIPAL DISPLAY PANEL
Principal Display Panel
NDC 55513-192-01
1 - Single Use Neulasta Prefilled Syringe
1 - Sterile On-body Injector for Neulasta
AMGEN®
Neulasta® Onpro™ kit
(pegfilgrastim)
Pegylated Recombinant Methionyl Human Granulocyte Colony-Stimulating Factor
(PEG-r-metHuG-CSF) derived from E Coli
6 mg/0.6 mL*
6 mg/0.6 mL*
*Prefilled syringe contains 0.64 mL to deliver 6 mg/0.6 mL when used with on-body injector
For Subcutaneous Use Only
Carton Contents (intended to be dispensed as a unit):
1 sterile On-body Injector for Neulasta
1 Neulasta prefilled syringe labeled for use with on-body injector only
1 patient instructions for use
1 healthcare provider instructions for use, 1 package insert
1 reference guide
This Product Contains Dry Natural Rubber
Store at 2° to 8°C (36° to 46°F).
Do Not Freeze or Shake. Keep in Carton to Protect from Light.
Rx Only
Manufactured by Amgen Inc.
Thousand Oaks, CA 91320-1799
U.S. License No. 1080
INGREDIENTS AND APPEARANCE
NEULASTA
