Cosela Injection, Powder, Lyophilized, For Solution
Product Images NDC 73594-0101

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cosela (NDC 73594-0101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharmacosmos Therapeutics 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

Chemical Structure (Cos08 0000 01)

Chemical Structure (Cos08 0000 01)
Chemical structure diagram of trilaciclib, the active ingredient in COSELA injection, powder, lyophilized, for solution, 300 mg/20 mL by Pharmacosmos Therapeutics Inc.*
FDA Label Image

Principal Display Panel – 300 mg Carton Label (Cos08 0000 02)

Principal Display Panel – 300 mg Carton Label (Cos08 0000 02)
COSELA (trilaciclib) for injection 300 mg/vial lyophilized powder for intravenous infusion after reconstitution and dilution. The label includes dosage and storage instructions, barcodes, and distributor information for Pharmacosmos Therapeutics Inc. The vial contains a single dose with instructions to discard unused portions.*
FDA Label Image

Principal Display Panel – 300 mg Vial Label (Cos08 0000 03)

Principal Display Panel – 300 mg Vial Label (Cos08 0000 03)
Label for COSELA (trilaciclib) injection, 300 mg per vial, lyophilized powder for intravenous infusion after reconstitution and dilution. The single-dose vial is distributed by Pharmacosmos Therapeutics Inc. with NDC 73594-0101. The label includes storage instructions, discard unused portion guidance, and barcode with lot and expiration information space.*

* 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.