Fylnetra Injection
Product Images NDC 70121-1627

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Fylnetra (NDC 70121-1627). 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

Logo (Fylnetra Pegfilgrastim Pbbk Injection 1)

FDA Label Image

Figure K (Fylnetra Pegfilgrastim Pbbk Injection 10)

FDA Label Image

Figure L-stop (Fylnetra Pegfilgrastim Pbbk Injection 11)

FDA Label Image

Figure M (Fylnetra Pegfilgrastim Pbbk Injection 12)

FDA Label Image

Figure N (Fylnetra Pegfilgrastim Pbbk Injection 13)

Figure N (Fylnetra Pegfilgrastim Pbbk Injection 13)
This text just contains information about two words: "Sharps" and "Container". It is not possible to determine the context or any useful description without further information.*
FDA Label Image

Carton (Fylnetra Pegfilgrastim Pbbk Injection 14)

Carton (Fylnetra Pegfilgrastim Pbbk Injection 14)
This is a description of a medication called Fylnetra. It is a pegylated recombinant methionyl human granulocyte colony-stimulating factor derived from E. coli. It comes in a single-dose prefilled syringe with a needle guard and contains 6mg of pegfilgrastim-pbbk in a sterile, colorless to slightly yellow solution. The syringe should be refrigerated at 2°C to 8°C (36°F to 46°F) and is for subcutaneous use only. The NDC code for this medication is 70121-1627-1.*
FDA Label Image

Lidding (Fylnetra Pegfilgrastim Pbbk Injection 15)

Lidding (Fylnetra Pegfilgrastim Pbbk Injection 15)
Pegfigrastm-pbbx is an injection used for subcutaneous purposes only. It contains Pegylated Recombinant Methionyl Human Granulocyte Colony Stimulating Factor (PEG-r-metHuG-CSF) derived from E. coli. It is essential to store it in its original carton, refrigerated at 2°C to 8°C and not freeze or shake it. The medicine is in sterile solution and has no preservative. The manufacturer is Kashiv BioSciences, LLC, located in Piscat, NJ. The label doesn't indicate the dosage; thus directions should be sought from the prescribing information.*
FDA Label Image

Label (Fylnetra Pegfilgrastim Pbbk Injection 16)

Label (Fylnetra Pegfilgrastim Pbbk Injection 16)
NDC 70121-1627-1 is a prescription-only medication in the form of a single-dose pre-filled syringe known as Fylnetra 6mg/0.6 mL. The medication is intended for subcutaneous injection use only, and it contains pegf`grasjum pbbk). The manufacturer of this medication is Kashiv BioSciences, LLC with a production location in Piscataway, NJ 08854. The medication was revised on 05-2022-00 and has a Lot number as well as an expiration date in the format of YYYY-MM.*
FDA Label Image

Figure A (Fylnetra Pegfilgrastim Pbbk Injection 2)

FDA Label Image

Figure C (Fylnetra Pegfilgrastim Pbbk Injection 3)

FDA Label Image

Figure D (Fylnetra Pegfilgrastim Pbbk Injection 4)

FDA Label Image

Figure E (Fylnetra Pegfilgrastim Pbbk Injection 5)

FDA Label Image

Figure F (Fylnetra Pegfilgrastim Pbbk Injection 6)

FDA Label Image

Figure G-h (Fylnetra Pegfilgrastim Pbbk Injection 7)

FDA Label Image

Figure I (Fylnetra Pegfilgrastim Pbbk Injection 8)

FDA Label Image

Figure J (Fylnetra Pegfilgrastim Pbbk Injection 9)

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