Pravastatin Sodium Tablet
Product Images NDC 68788-8871

View Photos of 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 Pravastatin Sodium (NDC 68788-8871). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred 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

Pravastatin Sodium Structural Formula (Image 1)

Pravastatin Sodium Structural Formula (Image 1)
Chemical structure of pravastatin sodium, showing its molecular arrangement with various functional groups including hydroxyl, carboxylate, and methyl groups, consistent with the drug's active ingredient.*
FDA Label Image

1 (Image 2)

1 (Image 2)
A line graph showing survival distributions for coronary heart disease death or nonfatal myocardial infarction over 5 years since randomization. It compares the proportion of subjects without events between a placebo group and a pravastatin group, with pravastatin showing a higher proportion without events over time. The graph includes a logrank P-value of 0.0001.*
FDA Label Image

Pravastatin Sodium Tablets Usp 20mg (Image 4)

Pravastatin Sodium Tablets Usp 20mg (Image 4)
Label for Pravastatin Sodium Tablets USP 20 mg, a prescription oral tablet. The label shows the generic name, strength, and manufacturer (Teva Czech Industries), with storage instructions and cautionary statements. It includes dosing directions in English and Spanish, barcode, and space for lot, batch, expiration, and insurance details. The product is labeled by Preferred Pharmaceuticals Inc.*

* 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.