Chemical Structure (Lovastatin 01)
Lovastatin
Product Images NDC 53489-609
View Photos of Packaging, Regulatory Labels, and Product Appearance
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.
Figure 1 (Lovastatin 02)
Principal Display Panel (10 mg Tablet Bottle Label)
Description: This is the information about Lovastatin tablets. The tablets contain Lovastatin of USP 10mg. It is meant to be stored at room temperature between 25°C (77°F). The tablets should be kept in a tight, light-resistant container. The tablet has the mark "MP 532" on it.*
Principal Display Panel (20 mg Tablet Bottle Label)
This is a description of a medication called Lovastatin USP, which comes in a pack of 100 tablets. The medication is kept in a tight, light-resistant container and each tablet contains 20mg of Lovastatin. The tablets are marked with the identifier "MP 533". The storage temperature for this medication should be between 20-25 degrees Celsius (68-77 degrees Fahrenheit) and should be dispensed only by prescription.*
Principal Display Panel (40 mg Tablet Bottle Label)
This is a description of Lovastatin tablets, USP containing 40mg of the active ingredient per tablet. The tablets are packaged in a container that protects them from light and should be stored at room temperature. The product comes in a bottle of 100 tablets and is marked with the NDC number 53489. The tablet is debossed with the marking "MP 534".*
* 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.
