Recothrom
Product Images NDC 65293-006

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Recothrom (NDC 65293-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Medicines Company, 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

5,000 Units Ndc: 65293-006-41 For Topical Use Only (DO NOT INJECT RECOTHROM® THROMBIN, TOPICAL (RECOMBINANT) 5,000 units)

5,000 Units Ndc: 65293-006-41 For Topical Use Only (DO NOT INJECT RECOTHROM® THROMBIN, TOPICAL (RECOMBINANT) 5,000 units)
RECOTHROM Thrombin Topical (Recombinant) 5,000 units carton label by The Medicines Company. The label displays product name, strength, dosage form, NDC 65293-006-41, and a list of carton contents including a single-use vial, diluent syringe, needle-free transfer device, empty syringe, and syringe label. It states 'For Topical Use Only - Do Not Inject' and storage instructions at 2-25°C (36-77°F).*
FDA Label Image

20,000 Units Ndc: 65293-007-41 For Topical Use Only (DO NOT INJECT RECOTHROM® THROMBIN, TOPICAL (RECOMBINANT) 20,000 units)

20,000 Units Ndc: 65293-007-41 For Topical Use Only (DO NOT INJECT RECOTHROM® THROMBIN, TOPICAL (RECOMBINANT) 20,000 units)
RECOTHROM Thrombin Topical (Recombinant) 20,000 units carton label showing product name, strength, and dosage form. It includes directions for topical use only and not for injection. The label specifies store conditions and contents of the single-use vial, with manufacturer information from The Medicines Company.*

* 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.