Lovastatin Tablet
Product Images NDC 68071-3261

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lovastatin (NDC 68071-3261). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (68071 3261 09 L39)

Label for Lovastatin 20 mg tablets by NuCare Pharmaceuticals, Inc. The label indicates a supply of 90 tablets. It includes the NDC 68071-3261-9, lot number 000000, and an expiration date placeholder 00-00. The label describes each tablet as a circular light green tablet debossed with 'LU' on one side and 'G02' on the other. Storage instructions and a warning to keep out of reach of children are also present.*

FDA Label Image

Lovastatin (C210d38a 1a95 4b40 Bb2e E627d15e7be9 01)

Chemical structure of lovastatin, a molecule characterized by multiple rings including a lactone and several hydrocarbon side chains, along with hydroxyl and carbonyl functional groups.*

FDA Label Image

Figure 1 (C210d38a 1a95 4b40 Bb2e E627d15e7be9 02)

A line graph titled 'Acute Major Coronary Events (Primary Endpoint)' showing the proportion of participants without event over years of follow-up. The graph compares two groups labeled Lovastatin and Placebo, indicating a 37% risk reduction with Lovastatin (p<0.0001). The x-axis represents years of follow-up from 0 to 6, and the y-axis shows the proportion of participants without event from 0.90 to 1.00.*

* 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.