Atorvastatin Calcium
Product Images NDC 67296-1422

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Atorvastatin Calcium (NDC 67296-1422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

30 Count Label (67296 1422 3)

30 Count Label (67296 1422 3)
Atorvastatin Calcium 20 mg packaging label showing a 30-tablet count. The label includes drug name, strength, quantity, lot number C03659X1, expiration date 09/22, and storage instructions. Manufactured by Sun Pharmaceutical Industries Limited in Mohali, India, and distributed by Redpharm Drug, Inc. in Eden Prairie, MN. The label also features a barcode and QR code.*
FDA Label Image

Structure (Image 01)

Structure (Image 01)
Chemical structure of Atorvastatin Calcium showing its molecular arrangement including aromatic rings, hydroxyl groups, fluorine substitution, and calcium ions.*
FDA Label Image

Figure1 (Image 02)

Figure1 (Image 02)
A line graph comparing cumulative incidence percentages over time (years) between Atorvastatin and Placebo groups. The graph shows separate curves for Atorvastatin (solid line) and Placebo (dashed line) over a 3.5-year period, illustrating differences in cumulative incidence rates.*
FDA Label Image

Figure 2 (Image 03)

Figure 2 (Image 03)
A Kaplan-Meier cumulative hazard curve comparing atorvastatin and placebo groups over four years of follow-up. The x-axis shows time to first primary endpoint in years, and the y-axis shows cumulative hazard percentage. The graph includes a hazard ratio (HR 0.63) with confidence interval and p-value indicating statistical significance.*
FDA Label Image

Figure 3 (Image 04)

Figure 3 (Image 04)
A line graph showing the percentage of subjects experiencing a cardiovascular event over time, comparing Atorvastatin 10 mg and Atorvastatin 80 mg doses. The horizontal axis represents time to first major cardiovascular endpoint in years, and the vertical axis shows the percentage of affected subjects, with hazard ratio and significance values noted.*
FDA Label Image

Spl-atorva-label1 (Spl Atorva Label1)

Spl-atorva-label1 (Spl Atorva Label1)
Atorvastatin Calcium Tablets, USP 10 mg label from Sun Pharma packaged in a blister of 90 tablets. The label includes the Rx only designation and manufacturer details, featuring a yellow box highlighting the strength. The branding of Sun Pharma appears below the tablet count.*
FDA Label Image

Spl-atorva-label2 (Spl Atorva Label2)

Spl-atorva-label2 (Spl Atorva Label2)
Atorvastatin Calcium Tablets USP 20 mg label displaying dosage strength and quantity of 90 tablets. The label includes the manufacturer Sun Pharma logo, directions indicating prescription use only, barcodes, and manufacturing details. It states the product is film-coated and provides storage and usage instructions.*
FDA Label Image

Spl-atorva-label3 (Spl Atorva Label3)

Spl-atorva-label3 (Spl Atorva Label3)
Atorvastatin Calcium Tablets USP 40 mg label displaying the product name, strength, and dosage form. The label indicates the package contains 90 tablets and includes manufacturer details for Sun Pharma with barcode and NDC 63304-829-90. The label also notes the prescription-only status and has a non-varnish area marked.*
FDA Label Image

Spl-atorva-label4 (Spl Atorva Label4)

Spl-atorva-label4 (Spl Atorva Label4)
Label for Atorvastatin Calcium Tablets, USP 80 mg by Sun Pharma, containing 90 tablets. The label includes dosage information, barcode, NDC number 63304-830-90, and manufacturing details. It is marked Rx only and features instructions to see the package insert for full dosage information.*

* 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.