Atorvastatin Calcium
Product Images NDC 76519-1084

3 FDA label images from H. J. Harkins Company Inc. · 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 Atorvastatin Calcium (NDC 76519-1084). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H. J. Harkins Company Inc., 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

Table Atorvastatin.jpg (Table Atorvastatin)

Table Atorvastatin.jpg (Table Atorvastatin)
A data table showing the effect of co-administered drugs on the pharmacokinetics of Atorvastatin. It details various drugs, doses, and the fold or percentage change in Atorvastatin's AUC and Cmax values during co-administration. Additional notes explain clinical significance, dose considerations, and effects of grapefruit juice and rifampin.*
FDA Label Image

Ator 80mg.jpg (Ator 80mg)

Ator 80mg.jpg (Ator 80mg)
Chemical structure diagram of the active ingredient atorvastatin calcium, showing its molecular arrangement including aromatic rings, hydroxyl groups, and calcium ion association as part of the compound.*
FDA Label Image

Atorvas 80mg.jpg (Atorvas 80mg)

Atorvas 80mg.jpg (Atorvas 80mg)
Label for ATORVASTATIN CALCIUM 80 mg tablets, produced by H.J. Harkins Company Inc. The label includes multiple sections with the product name, strength, dosage form, NDC number 76519-1084-XX, manufacturer NDC 69097-0911-05, lot number B155018, and expiration date 09/30/18. The label also contains dispensing cautions and storage instructions, and a note to take the medication as directed by a physician.*

* 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.