Pravastatin Sodium
Product Images NDC 70934-832

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 70934-832). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Label (70934 832 90 Master Bottle Label Approval Rev A 03 21)

Label (70934 832 90 Master Bottle Label Approval Rev A 03 21)
Label for Pravastatin Sodium Tablets, USP 40 mg by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates a package of 90 tablets, Rx only, with storage instructions and a note to see the package insert for dosage information. The label includes the NDC number 70934-832-90.*
FDA Label Image

Img-1 (Img 1)

Img-1 (Img 1)
A line graph titled 'Coronary Heart Disease Death or Nonfatal Myocardial Infarction Survival Distributions' compares the proportion of subjects without event over approximately 5 years since randomization between Placebo and Pravastatin groups. The y-axis represents the proportion of subjects without event, ranging from 0.9 to 1, and the x-axis represents years since randomization, from 0 to 5. The graph shows two survival curves, with the Pravastatin group having a lower proportion free of event compared to Placebo as time progresses, and a statistical significance indicated by Logrank P = 0.0001.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of pravastatin sodium, showing its molecular formula C23H35NaO7 and molecular weight 446.52.*

* 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.