Pravastatin Sodium Tablet
Product Images NDC 61919-708

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pravastatin Sodium (NDC 61919-708). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

708-30 (708 30)

Label for PRAVASTATIN SODIUM 40 mg, a 30-tablet bottle package. Generic for Pravachol, each uncoated tablet contains Pravastatin Sodium USP 40 mg. Packaged and distributed by Direct_Rx, information includes lot and expiration date details along with NDC numbers.*

FDA Label Image

801 90

Label for PRAVASTATIN SODIUM 20 mg, 90 tablets, generic for PRAVACHOL. The label states the active ingredient as pravastatin sodium 20 mg and includes FDA-required disclaimers and storage instructions. Packaged and distributed by Direct_Rx, with lot number 07FE1911 and expiration date 05/31/20. The label also includes warnings about possible side effects such as headaches, nausea, fever, hives, difficulty breathing, or swallowing.*

* 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.