Lovastatin Tablet
Product Images NDC 50090-0759

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lovastatin (NDC 50090-0759). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

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Chemical structure of lovastatin, showing its molecular arrangement with hydroxyl, carbonyl, and methyl groups in a complex fused ring system.*

FDA Label Image

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A line graph titled 'Acute Major Coronary Events (Primary Endpoint)' showing the proportion of participants without events over time in years of follow-up. Two lines compare Lovastatin and placebo, illustrating a 37% risk reduction with Lovastatin (p<0.0001). The y-axis represents the proportion of participants without events, and the x-axis represents years of follow-up.*

FDA Label Image

Label Image (Lbl500900759)

Lovastatin 20 mg oral tablets packaging label from A-S Medication Solutions. The label shows the product name, strength of 20 mg per tablet, quantity of 30 tablets, and storage instructions to store at 77 degrees F and protect from light. The label includes a QR code, lot number, and product number details.*

FDA Label Image

Label Image (Lbl500900762)

Lovastatin 40 mg oral tablets label from A-S Medication Solutions. The label displays the product name Lovastatin with strength 40 mg, dosage form as tablets, and package size of 30 tablets. Storage instructions indicate to store at 77 degrees Fahrenheit and protect from light. It includes the NDC number 50090-0762-0 and a note that each tablet contains lovastatin USP 40 mg.*

* 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.