Stimufend Injection, Solution
Product Images NDC 65219-371

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 21 technical images submitted to the FDA as part of the official labeling for Stimufend (NDC 65219-371). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi 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.

FDA Label Image

Fresenius Kabi Logo (Sti04 0001 01)

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Figure A (Sti04 0001 02)

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Figure B (Sti04 0001 03)

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Figure C (Sti04 0001 04)

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Figure D (Sti04 0001 05)

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Figure E (Sti04 0001 06)

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Figure F (Sti04 0001 07)

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Figures G And H (Sti04 0001 08)

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Figure I (Sti04 0001 09)

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Figure J (Sti04 0001 10)

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Figure K (Sti04 0001 11)

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Figure L (Sti04 0001 12)

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Figure M (Sti04 0001 13)

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Figures N And O (Sti04 0001 14)

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Figure P (Sti04 0001 15)

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Figure Q (Sti04 0001 16)

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Figure R (Sti04 0001 17)

FDA Label Image

Fresenius Kabi Logo (Sti04 0001 18)

FDA Label Image

Package Label – Principal Display – Stimufend –one 0.6 mL Single-dose Prefilled Syringe Carton Panel (Sti04 0001 19)

FDA Label Image

Package Label – Principal Display – Stimufend – 0.6 mL Single-dose Prefilled Syringe Blister Pack Label (Sti04 0001 20)

Package Label – Principal Display – Stimufend – 0.6 mL Single-dose Prefilled Syringe Blister Pack Label (Sti04 0001 20)
Fresenius Kabi's StimuFend is a subcutaneous injection containing Pegylated Recombinant Methionyl Human Granulocyte Colony Stimulating Factor, used to treat low white blood cell count. It is stored refrigerated, protected from light, and is contained in a pre-filled syringe. This product is manufactured by Fresenius Kabi USA and has no U.S. standard potency. The given text contains necessary information about the product, precautions, and its manufacturing details.*
FDA Label Image

Package Label – Principal Display – Stimufend – 0.6 mL Single-dose Prefilled Syringe Label (Sti04 0001 21)

Package Label – Principal Display – Stimufend – 0.6 mL Single-dose Prefilled Syringe Label (Sti04 0001 21)
Stimufend' is an injection medication with the active ingredient pegfilgrastim=fpgk. It is U.S. licensed with the number 2146 and produced by Fresenius Kabi USA LLC. The dosage and usage instructions are not available.*

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