Pravastatin Sodium Tablet
Product Images NDC 0480-7270

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pravastatin Sodium (NDC 0480-7270). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva 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

1 (Image 1)

FDA Label Image

2 (Image 2)

This is a survival distribution chart that compares the effectiveness of a placebo versus Pravastatin in preventing coronary heart disease-related death or nonfatal myocardial infarction. The chart shows the proportion of subjects that did not experience an event over a five-year period since randomization. The results yielded a Lagrank P value of less than 0.0001.*

FDA Label Image

90 Count (Image 3)

This is a description of Pravastatin Sodium Tablets, USP, which come in a bottle of 90 tablets. Each tablet contains 80 mg of pravastatin sodium, USP. The product has a unique identification code - NDC 0480-7270-98 and GTIN 0304807270988. The tablets should be stored at controlled room temperature and protected from moisture and light. The product is manufactured in the Czech Republic by Teva Czech Industries and distributed by Teva Pharmaceuticals in Parsippany, NJ. The medication is prescription-only, and the bottle includes a serialization coding area. Keep out of reach of children.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.