Vabysmo Injection, Solution
Product Images NDC 50242-096

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Vabysmo (NDC 50242-096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genentech, 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 A (Faricimab 01)

FDA Label Image

Figure B (Faricimab 02)

FDA Label Image

Figure C (Faricimab 03)

FDA Label Image

Figure D (Faricimab 04)

FDA Label Image

Figure E (Faricimab 05)

FDA Label Image

Figure F (Faricimab 06)

FDA Label Image

Figure G (Faricimab 07)

FDA Label Image

Figure H (Faricimab 08)

FDA Label Image

Figure I (Faricimab 09)

FDA Label Image

Figure J (Faricimab 10)

FDA Label Image

Figure K (Faricimab 11)

FDA Label Image

Figure L (Faricimab 12)

FDA Label Image

Figure 1 (Faricimab 13)

Figure 1 (Faricimab 13)
The text describes the mean change in BCVA (a visual acuity measurement) in ETDRS letters over a period of a few weeks in a study where one group received VABYSMO (458 individuals) and another received Afbercept (451 individuals). Unfortunately, no further information is available.*
FDA Label Image

Figure 2 (Faricimab 14)

FDA Label Image

Figure 3 (Faricimab 15)

FDA Label Image

Figure 4 (Faricimab 16)

FDA Label Image

Principal Display Panel (6 mg Vial Carton)

Principal Display Panel (6 mg Vial Carton)
This text is a description of a medication for intravitreal injection. The medication is called "faricimab-svoa" and is contained in a single-dose vial. The vial contains 6mg of the medication, which is a 0.05mL solution of 120mg/mL. The package includes one single-dose vial and one transfer filter needle from Genentech. The user is advised to discard any unused portion. The National Drug Code (NDC) for the medication is 50242-096-01.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.