Romidepsin Kit
Product Images NDC 70771-1986

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Romidepsin (NDC 70771-1986). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Label (4dea32df 60fe 4f7b 8a94 45266b13553e 01)

Label for Romidepsin for Injection 10 mg/vial, a sterile single-dose vial kit for intravenous use only by Zydus Lifesciences Limited. Instructions for reconstitution and dilution are included, with storage recommendations between 20°C to 25°C. The label includes active and inactive ingredients, lot and expiration placeholders, and a barcode.*

FDA Label Image

Diluent Label (4dea32df 60fe 4f7b 8a94 45266b13553e 02)

Label for Romidepsin Diluent kit by Zydus Lifesciences Limited, containing 2.2 mL per single-dose vial. The label includes storage instructions (20°C to 25°C, excursions 15°C to 30°C), mentions the diluent composition (80% propylene glycol and 20% dehydrated alcohol), and dosage instructions for reconstituting a 10 mg vial of Romidepsin for injection. The product is sterile and prescription only.*

FDA Label Image

Kit Label (4dea32df 60fe 4f7b 8a94 45266b13553e 03)

Packaging label for Romidepsin for Injection Kit, 10 mg per vial, for intravenous use. The label indicates the kit contains one 10 mg single-dose vial of Romidepsin and one single-dose vial with 2.2 mL of diluent. Directions include reconstitution and dilution instructions. The product is sterile, single-dose, and for prescription use only. Manufactured by Zydus Lifesciences Limited.*

* 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.