Atorvastatin Calcium Tablet, Film Coated
Product Images NDC 42385-941

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Atorvastatin Calcium (NDC 42385-941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laurus Labs Limited, 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

Figure1 (Atorvastatin Figure1)

A line chart showing the effect of Atorvastatin 10 mg/day on cumulative incidence of non-fatal myocardial infarction or coronary heart disease death over approximately 3.5 years. The chart compares Atorvastatin (solid line) versus placebo (dashed line) with cumulative incidence (%) on the y-axis and years on the x-axis. Hazard ratio and p-value are also indicated below the x-axis.*

FDA Label Image

Figure10 (Atorvastatin Figure10)

Label for Atorvastatin Calcium Tablets, USP 40 mg, film-coated oral tablets. The package contains 30 tablets and is manufactured by Laurus Labs Limited, India, for Laurus Generics Inc., Berkeley Heights, NJ. The label includes dosage strength, storage instructions, and states Rx only.*

FDA Label Image

Figure11 (Atorvastatin Figure11)

Packaging label for Atorvastatin Calcium Tablets, USP 40 mg by Laurus Labs Limited. The label shows a box containing 100 (10 x 10) unit-dose tablets for oral use, marked for in-institution use only. It includes manufacturing details for Laurus Generics Inc. and Laurus Labs Limited, as well as storage instructions and a barcode. The label displays the NDC number 42385-942-68 and indicates prescription-only (Rx Only) status.*

FDA Label Image

Figure12 (Atorvastatin Figure12)

Label sheet for Atorvastatin Calcium 40 mg tablets, USP, film-coated oral tablets. Each label features the drug name prominently with strength in blue, along with Rx Only, NDC 42385-942-10, manufacturer Laurus Labs Limited, and a barcode. The sheet contains multiple identical labels arranged in a grid.*

FDA Label Image

Figure13 (Atorvastatin Figure13)

Label for Atorvastatin Calcium Tablets, USP 80 mg film-coated tablets. The label states the quantity as 30 tablets, manufactured by Laurus Labs Limited, with Laurus Generics Inc. as the labeler. It includes storage instructions and NDC 42385-943-30. The label specifies prescription use only.*

FDA Label Image

Figure14 (Atorvastatin Figure14)

Packaging label for Atorvastatin Calcium Tablets, USP 80 mg by Laurus Labs Limited. The label indicates 64 unit-dose tablets (8 x 8), marked for in-institution use only and Rx only. It lists storage conditions and manufacturer details for Laurus Generics Inc. and Laurus Labs Limited, with an NDC of 42385-943-64.*

FDA Label Image

Figure15 (Atorvastatin Figure15)

Atorvastatin Calcium Tablet, USP 80 mg labels arranged in a sheet of eight. Each label includes the Rx Only designation, NDC 42385-943-08, bar code, strength prominently displayed as 80 mg, and manufacturer Laurus Labs Limited. The labels are intended for film-coated oral tablets.*

FDA Label Image

Figure16 (Atorvastatin Figure16)

Packaging label for Atorvastatin Calcium Tablets, USP 80 mg by Laurus Labs Limited. The box contains 100 unit-dose film-coated tablets (10 x 10) intended for in-institution use only. The label includes storage information, manufacturer and distributor details, and the NDC number 42385-943-68. The design features the Laurus Labs logo and emphasizes the 80 mg strength prominently.*

FDA Label Image

Figure17 (Atorvastatin Figure17)

A sheet containing multiple identical white labels for Atorvastatin Calcium 80 mg tablets. Each label includes the text 'Rx Only', the NDC code 42385-943-10, 'Atorvastatin Calcium Tablet, USP', and the strength in a brown box marked '80 mg'. Manufacturer information states 'Mfd. by: Laurus Labs Limited' along with a manufacturing license number. Each label also features a barcode.*

FDA Label Image

Figure2 (Atorvastatin Figure2)

A line graph depicting the effect of Atorvastatin 10 mg/day versus placebo on cumulative hazard percentage over time, measured in years, for major cardiovascular events in the CARDS study. The x-axis represents time in years through four years of follow-up, and the y-axis shows cumulative hazard percentage. The graph compares two lines: a dashed line for placebo and a solid line for Atorvastatin, showing lower cumulative hazard with Atorvastatin over time.*

FDA Label Image

Figure3 (Atorvastatin Figure3)

A line graph titled 'Effect of Atorvastatin 80 mg/day vs. 10 mg/day on Time to Occurrence of Major Cardiovascular Events.' It shows the percentage of subjects experiencing events over time in years. Two lines represent Atorvastatin 10 mg (dashed) and 80 mg (solid), with the 80 mg line showing a lower event rate over 5 years. The graph includes a hazard ratio (HR 0.78) with confidence intervals and a p-value.*

FDA Label Image

Figure4 (Atorvastatin Figure4)

Atorvastatin Calcium Tablets, USP 10 mg film-coated tablet label. The label indicates 30 tablets per container, manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. The label includes storage instructions, dosage reference, and the NDC 42385-940-30 with a barcode.*

FDA Label Image

Figure5 (Atorvastatin Figure5)

Packaging label for Atorvastatin Calcium Tablets, USP 10 mg by Laurus Labs Limited. The label shows the product as film-coated tablets in a unit-dose format, with a package size of 100 tablets (10 x 10). It includes dosing strength prominently in blue, states 'For in-institution use only,' and lists Laurus Generics Inc. as the manufacturer. Storage instructions and an NDC number 42385-940-68 are also visible.*

FDA Label Image

Figure6 (Atorvastatin Figure6)

Sheet of 10 mg Atorvastatin Calcium tablet labels. Each label states Rx Only, NDC 42385-940-10, Atorvastatin Calcium Tablet, USP with strength 10 mg in blue box. Manufactured by Laurus Labs Limited with manufacturing license number 16/VSP/AP/2015/F&B/CC. Each label includes a barcode. Labels are arranged in two columns and five rows on a white background.*

FDA Label Image

Figure7 (Atorvastatin Figure7)

Atorvastatin Calcium 20 mg film-coated tablets label displaying the strength prominently in a red box. The label includes tablet quantity of 30, manufacturer Laurus Labs Limited, and distributor Laurus Generics Inc., with storage instructions and dosage guidance text. The tablet is an oral prescription drug.*

FDA Label Image

Figure8 (Atorvastatin Figure8)

The image shows the packaging label for Atorvastatin Calcium Tablets, USP, 20 mg strength, manufactured by Laurus Labs Limited. The label indicates the product contains 100 unit-dose tablets (10 x 10) and is for in-institution use only. It includes storage instructions and manufacturer information, featuring the Laurus Labs logo and an NDC code 42385-941-68.*

FDA Label Image

Figure9 (Atorvastatin Figure9)

This image shows a sheet of Atorvastatin Calcium Tablet, USP labels. Each label indicates a strength of 20 mg, states 'Rx Only,' and includes the NDC number 42385-941-10. The manufacturer is Laurus Labs Limited, with a manufacturing lot number referenced. Each label contains a barcode on the right side.*

FDA Label Image

Atorvastatin-structure (Atorvastatin Structure)

Chemical structure of atorvastatin calcium showing two atorvastatin molecules complexed with one calcium ion and three water molecules as hydrate. The structure includes phenyl rings, fluorophenyl, and functional groups characteristic of atorvastatin.*

* 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.