Pravastatin Sodium Tablet
Product Images NDC 71610-637

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pravastatin Sodium (NDC 71610-637). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Bottle Label 80 mg (71610 0637 30)

Bottle Label 80 mg (71610 0637 30)
PRAVASTATIN SODIUM USP 80 mg oral tablet label with package size of 30 tablets. The label includes NDC 71610-0637-30, storage instructions, manufacturer listed as Apotex Inc. in Toronto, Canada, and packaging by Aphena Pharma Solutions in Cookeville, TN. It specifies the product is RX only.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Pravastatin-fig1 (Pravastatin Fig1)

Pravastatin-fig1 (Pravastatin Fig1)
A Kaplan-Meier survival curve showing the proportion of subjects without coronary heart disease death or nonfatal myocardial infarction over a period of 5 years. Two lines represent groups receiving placebo and pravastatin, with survival distributions compared using a Logrank test (P = 0.0001). The x-axis is labeled 'Years Since Randomization' and the y-axis is labeled 'Proportion of Subjects Without Event.'*
FDA Label Image

Pravastatin-structure (Pravastatin Structure)

Pravastatin-structure (Pravastatin Structure)
Chemical structure of pravastatin sodium, showing its molecular formula C23H35NaO7 and molecular weight 446.52. The diagram illustrates the arrangement of atoms in the molecule.*

* 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.