Rosuvastatin Tablet, Film Coated
Product Images NDC 51407-848

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Rosuvastatin (NDC 51407-848). 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

51407-848-90lb (Rosuvastatin)

51407-848-90lb (Rosuvastatin)
Label for Rosuvastatin 5 mg film-coated tablets, USP, produced by Golden State Medical Supply, Inc. The label indicates a package size of 90 tablets with NDC 51407-848-90. It includes dosage information referencing the prescribing information, storage instructions, and safety warnings such as keeping out of reach of children. The label features a barcode and the GSMS Incorporated logo.*
FDA Label Image

51407-849-90lb (Rosuvastatin)

51407-849-90lb (Rosuvastatin)
Label for Rosuvastatin 10 mg film-coated tablets, USP, from Golden State Medical Supply, Inc. The label shows a package size of 90 tablets for oral use. It includes dosage strength prominently in a blue box, the NDC number 51407-849-90, and a barcode. Storage instructions and dispensing guidelines are also displayed.*
FDA Label Image

51407-850-90lb (Rosuvastatin)

51407-850-90lb (Rosuvastatin)
Label for Rosuvastatin 20 mg film-coated tablets, USP, marketed by Golden State Medical Supply, Inc. The package contains 90 tablets. The label includes the NDC code 51407-850-90 and instructions for storage at 20°-25°C, dispensing patient information, and keeping medication out of children's reach. Barcode and QR code are present.*
FDA Label Image

51407-851-90lb (Rosuvastatin)

51407-851-90lb (Rosuvastatin)
Label for Rosuvastatin 40 mg film-coated tablets by Golden State Medical Supply, Inc. The label includes the NDC number 51407-851-90 and indicates a package size of 90 tablets. Storage instructions specify controlled room temperature. The label also contains pharmacist dispensing instructions and a barcode.*
FDA Label Image

Figure-01 (Figure 1)

Figure-01 (Figure 1)
A Kaplan-Meier curve showing cumulative incidence percentage over years for Rosuvastatin versus placebo groups. The solid line represents Rosuvastatin, and the dotted line represents placebo. The graph includes hazard ratio (HR 0.56 with 95% CI 0.46-0.69) and a p-value <0.001. Below the x-axis is a risk table with the number of subjects at risk for each group (RSV and placebo) at different time points over 5 years.*
FDA Label Image

Figure-02 (Figure 2)

Figure-02 (Figure 2)
A table presenting clinical event rates comparing Rosuvastatin 20 mg and placebo 20 mg groups across various endpoints, including primary endpoint (MCE), cardiovascular death, nonfatal stroke, nonfatal myocardial infarction (MI), hospitalized unstable angina, and arterial revascularization. It includes number of events, hazard ratios with 95% confidence intervals, and p-values, accompanied by a hazard ratio plot for visual comparison.*
FDA Label Image

Figure-02 (Figure 3)

Figure-02 (Figure 3)
A box plot chart comparing the percent change from baseline in LDL-C levels for Rosuvastatin, Atorvastatin, Simvastatin, and Pravastatin at various doses (mg). The y-axis shows percent change from 0 to -75%, and the x-axis lists doses for each statin drug, illustrating variations in LDL-C reduction across the different medications and strengths.*
FDA Label Image

Structural Formula (Rosuvastatin Str)

Structural Formula (Rosuvastatin Str)
Chemical structure of rosuvastatin calcium, the active ingredient in Rosuvastatin tablets. The diagram shows the molecular arrangement with annotated functional groups and the calcium ion association.*

* 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.