Romidepsin Injection, Solution, Concentrate
Product Images NDC 70121-2250

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 Romidepsin (NDC 70121-2250). 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

1 (Romidepsin Injection 1)

1 (Romidepsin Injection 1)
Chemical structure of romidepsin, illustrating the molecular arrangement of the active ingredient with its characteristic cyclic peptide framework and disulfide bonds as depicted in the black-and-white diagram.*
FDA Label Image

Label (Romidepsin Injection 2)

Label (Romidepsin Injection 2)
Romidepsin Injection 27.5 mg/5.5 mL (5 mg/mL) solution concentrate for intravenous infusion. Single-dose vial, sterile. Contains romidepsin with excipients including povidone, DL-alpha tocopherol, dehydrated alcohol, and propylene glycol. Label shows dilution and usage instructions, storage conditions, and distribution by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Made in India.*
FDA Label Image

Carton (Romidepsin Injection 3)

Carton (Romidepsin Injection 3)
Packaging label for Romidepsin Injection 5 mg/mL (27.5 mg/5.5 mL) concentrate for intravenous infusion. The label includes dosage instructions, storage information, and cautions that it is a cytotoxic agent. Manufactured by Amneal Oncology Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. The label shows product NDC 70121-2250-1 and includes barcodes and batch coding area.*

* 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.