Pravastatin Sodium Tablet
Product Images NDC 61919-708

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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.

Product Images & Figures Index

FDA Label Image

708-30 (708 30)

708-30 (708 30)
This is a description of a medication called Pravastatin Sodium. It comes in the form of an uncoated tablet that contains 40mg of Pravastatin Sodium USP. The medication is used to lower cholesterol levels and is the generic version of Pravachol. The text includes dosage instructions, the NDC (National Drug Code) number, and the lot number and expiry date of the medication. The text also includes warnings, such as the prohibition of transferring the drug to anyone other than the patient for whom it was prescribed and the need to keep it out of reach of children. The medication may cause side effects such as headaches, fever, hives, difficulty swallowing, nausea, and difficulty breathing.*
FDA Label Image

801 90

801 90
Pravastatin Sodium 20mg is a medication used to lower cholesterol levels in the body. It is available in tablet form and is sold in a bottle of 90 tablets per pack. The tablets contain pravastatin sodium USP, with each tablet containing 20mg of the active ingredient. The manufacturer's name, production code, and expiration date details are also included on the label. The medication is packaged and distributed by an unnamed company located in the United States.*

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