Pravastatin Sodium
Product Images NDC 53808-0685

3 FDA label images from State Of Florida Doh Central Pharmacy · 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 53808-0685). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Label Image For 10mg (Pravastatin Sodium 10mg)

Label Image For 10mg (Pravastatin Sodium 10mg)
Label for Pravastatin Sodium 10 mg tablets, quantity 30, with lot number ML9367 and expiration date 04/30/2013. The product is prescription only (Rx Only) and labeled by the DOH Central Pharmacy, Tallahassee, FL. The label includes a barcode and UPC number 368382070050.*
FDA Label Image

Pravastatin Sodium Tablets, Usp (Pravastatinnatabsusp Figure 01)

Pravastatin Sodium Tablets, Usp (Pravastatinnatabsusp Figure 01)
Chemical structure diagram of pravastatin sodium displaying its molecular formula C23H35NaO7 and molecular weight 446.52.*
FDA Label Image

Pravastatin Sodium Tablets, Usp (Pravastatinnatabsusp Figure 02)

Pravastatin Sodium Tablets, Usp (Pravastatinnatabsusp Figure 02)
A line graph titled 'Coronary Heart Disease Death or Nonfatal Myocardial Infarction Survival Distributions' displaying two survival curves for Placebo and Pravastatin groups over 5 years since randomization. The y-axis shows the proportion of subjects without event, and the graph includes a Logrank P value of 0.0001, indicating statistical comparison of the survival distributions.*

* 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.