Ezetimibe And Simvastatin Tablet
Product Images NDC 51407-191

7 FDA label images from Golden State Medical Supply, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ezetimibe And Simvastatin (NDC 51407-191). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-190-30lb (EZETIMIBE SIMVASTATIN 10MG10MG TABS.jpg)

51407-190-30lb (EZETIMIBE SIMVASTATIN 10MG10MG TABS.jpg)
Label for Ezetimibe and Simvastatin tablets 10 mg/10 mg by Golden State Medical Supply, Inc. The label indicates a package of 30 tablets, includes the National Drug Code (NDC) 51407-190-30, and features storage instructions and a prescription-only (Rx only) designation. Manufacturer information and barcode are also visible.*
FDA Label Image

51407-191-30lb (EZETIMIBE SIMVASTATIN 10MG20MG TABS.jpg)

51407-191-30lb (EZETIMIBE SIMVASTATIN 10MG20MG TABS.jpg)
Label for Ezetimibe and Simvastatin tablets, strength 10 mg/20 mg, in a package of 30 tablets. The label includes the NDC number 51407-191-30 and states that the product is for prescription use only (Rx only). Storage instructions specify to keep at 20° to 25°C. The labeler is Golden State Medical Supply, Inc.*
FDA Label Image

51407-192-30lb (EZETIMIBE SIMVASTATIN 10MG.jpg)

51407-192-30lb (EZETIMIBE SIMVASTATIN 10MG.jpg)
Label for Ezetimibe and Simvastatin tablets, strength 10 mg/40 mg, in a 30-tablet package. The label indicates the product is prescription only (Rx only) and includes storage instructions at 20° to 25°C (68° to 77°F). The labeler is Golden State Medical Supply, Inc., with manufacturing attributed to Dr. Reddy's Laboratories, LA LLC, Camarillo, CA. The National Drug Code (NDC) is 51407-192-30.*
FDA Label Image

51407-193-30lb (EZETIMIBE SIMVASTATIN 10MG80MG TABS.jpg)

51407-193-30lb (EZETIMIBE SIMVASTATIN 10MG80MG TABS.jpg)
Label for Ezetimibe and Simvastatin tablets, 10 mg/80 mg strength, containing 30 tablets. The label includes the NDC number 51407-193-30 and states the product is a prescription drug by Golden State Medical Supply, Inc. Storage instructions to keep at 20° to 25°C are visible, along with warnings to keep out of reach of children and directions to see package insert for dosage information.*
FDA Label Image

Ezetimibe Structural Formula (Image 01)

Ezetimibe Structural Formula (Image 01)
Chemical structure of ezetimibe and simvastatin, showing molecular bonds and functional groups characteristic of these active ingredients.*
FDA Label Image

Simvastatin Structural Formula (Image 02)

Simvastatin Structural Formula (Image 02)
Chemical structure of the active ingredient in Ezetimibe and Simvastatin combination drug, showing molecular bonds and functional groups in a black-and-white line drawing format.*
FDA Label Image

Figure 1 Effect Of Ezetimibe And Simvastatin On The Primary Endpoint Of Risk Of Major Vascular Events (Image 03)

Figure 1 Effect Of Ezetimibe And Simvastatin On The Primary Endpoint Of Risk Of Major Vascular Events (Image 03)
A line graph showing major vascular events over 5 years of follow-up comparing patients treated with Ezetimibe and Simvastatin versus placebo. The y-axis represents the percentage of patients with events, and the x-axis shows years of follow-up. The graph indicates fewer events for the Ezetimibe and Simvastatin group, with a statistically significant difference (Logrank P=0.001). Patient numbers at risk for both groups are listed below the graph.*

* 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.