Lovastatin
Product Images NDC 53489-609

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lovastatin (NDC 53489-609). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mutual Pharmaceutical Company, 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

Chemical Structure (Lovastatin 01)

Chemical structure diagram of lovastatin showing its molecular arrangement with multiple rings and functional groups including hydroxyl, ketone, and methyl groups.*

FDA Label Image

Figure 1 (Lovastatin 02)

A line graph showing the proportion of participants without acute major coronary events over six years of follow-up, comparing Lovastatin and placebo groups. The graph indicates a 37% risk reduction for Lovastatin versus placebo with a p-value less than 0.001.*

FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Label for Lovastatin Tablets USP 10 mg by Mutual Pharmaceutical Company, Inc. The label indicates a package of 100 tablets with dosage strength of 10 mg. It includes storage instructions, a barcode, and the NDC 53489-607-01. The label also specifies the product is for prescription use only and mentions a light-resistant container.*

FDA Label Image

Principal Display Panel (20 mg Tablet Bottle Label)

Label for Lovastatin Tablets USP 20 mg from Mutual Pharmaceutical Company, Inc., Philadelphia, PA. The label states the package contains 100 tablets intended for oral use. Storage instructions recommend 20° to 25°C. The label includes an NDC number and a barcode.*

FDA Label Image

Principal Display Panel (40 mg Tablet Bottle Label)

Label for lovastatin tablets USP, 40 mg strength, supplied by Mutual Pharmaceutical Company, Inc. The label indicates a package of 100 tablets, stored in a light-resistant container, with temperature storage instructions of 20°C to 25°C (68°F to 77°F). The label includes the NDC code 53489-609-01 and shows the manufacturer location in Philadelphia, PA.*

* 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.