Vibativ Injection, Powder, Lyophilized, For Solution
Product Images NDC 66220-315

3 FDA label images from Cumberland Pharmaceuticals Inc. · 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 Vibativ (NDC 66220-315). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cumberland Pharmaceuticals 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

Figure 1 (Vib09 0001 01)

Figure 1 (Vib09 0001 01)
Chemical structure of telavancin hydrochloride showing its molecular arrangement, including multiple rings and side chains with chlorine atoms, hydroxyl groups, and hydrochloride ions (x HCl, where x is 1-3). The diagram is labeled with the generic drug name below.*
FDA Label Image

Principal Display Panel (750 mg/vial Carton Label)

Principal Display Panel (750 mg/vial Carton Label)
VIBATIV 750 mg vial packaging label for telavancin injection, lyophilized powder for solution, by Cumberland Pharmaceuticals Inc. The label shows a single-dose vial containing 750 mg of telavancin. It includes storage instructions, reconstitution guidelines to achieve 15 mg/mL concentration, and warnings to dispense with an enclosed Medication Guide. The design features the product name prominently with dosage information and company branding.*
FDA Label Image

Principal Display Panel (750 mg/vial Vial Label)

Principal Display Panel (750 mg/vial Vial Label)
Label for VIBATIV (telavancin) injection 750 mg/vial, a sterile, lyophilized, preservative-free powder for intravenous infusion. The label includes storage instructions, usage notes, and manufacturer information for Cumberland Pharmaceuticals Inc.*

* 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.