Lovastatin Tablet
Product Images NDC 63187-765

3 FDA label images from Proficient Rx Lp · 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 Lovastatin (NDC 63187-765). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Lovastatin (Lovastatintabusp Figure 01)

Lovastatin (Lovastatintabusp Figure 01)
Chemical structure of lovastatin, showing its molecular framework with labeled atoms and bonds typical of a statin compound.*
FDA Label Image

Figure 1 (Lovastatintabusp Figure 02)

Figure 1 (Lovastatintabusp Figure 02)
A line graph titled 'Acute Major Coronary Events (Primary Endpoint)' comparing the proportion of participants without event over years of follow-up between two groups: Lovastatin and Placebo. The Lovastatin group shows a higher proportion without events compared to Placebo, with a noted 37% risk reduction (p < 0.001). The x-axis represents years of follow-up (0 to 6+), and the y-axis represents the proportion of participants without events (0 to 1).*
FDA Label Image

63187-765-30 (Lovastatintabusp Figure 04)

63187-765-30 (Lovastatintabusp Figure 04)
Lovastatin 20 mg tablets label by Proficient Rx LP. The label indicates 30 tablets per package and states each tablet contains 20 mg lovastatin USP. Tablets are described as light green, circular, beveled edged, uncoated, with debossed markings 'LU' and 'G02'. The manufacturer is Lupin Limited, Goa, India. Storage instructions note keeping at 25°C and out of reach of children.*

* 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.