Quetiapine Fumarate Tablet
Product Images NDC 68180-449

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 68180-449). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Molecular Structure (156f500b 643d 4f44 9963 C65d2ec23f37 01)

Chemical structure of quetiapine fumarate, showing the molecular arrangement of the quetiapine moiety and the fumarate moiety, as presented in the FDA SPL submission for Lupin Pharmaceuticals, Inc. drug product.*

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Figure 1 (156f500b 643d 4f44 9963 C65d2ec23f37 02)

A line chart showing the proportion of patients with relapse (%) over time in weeks (0 to 100). Two curves compare QTP+LI/VAL and PLA+LI/VAL groups, with relapse proportions increasing over time. The PLA+LI/VAL group shows a higher relapse rate peaking near 70%, while the QTP+LI/VAL group peaks near 40%, as indicated in the legend.*

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Figure 2 (156f500b 643d 4f44 9963 C65d2ec23f37 03)

A line graph showing the proportion of patients with relapse (%) over time in weeks (0 to 100). Two groups are compared: QTP+LI/VAL (dashed line) and PLA+LI/VAL (solid line). The PLA+LI/VAL group shows a higher relapse proportion over time compared to QTP+LI/VAL.*

FDA Label Image

25 mg (100s)

Quetiapine Tablets USP 25 mg film-coated tablets label by Lupin Pharmaceuticals, Inc. The label includes the NDC 68180-445-01, a 100 tablet count, and dosage information. It also provides storage instructions, manufacturer details for Lupin Pharmaceuticals, Inc. in Baltimore and Lupin Limited in India, along with a barcode and QR code for medication guide access.*

FDA Label Image

50 mg (100s)

Label of Quetiapine Tablets USP 50 mg, oral tablets packaged in a container of 100 count. The label includes NDC 68180-446-01, states each film-coated tablet contains 57.56 mg quetiapine fumarate USP equivalent to 50 mg quetiapine, and directs pharmacists to dispense the medication guide. Manufactured by Lupin Pharmaceuticals, Inc., Baltimore, MD, and Lupin Limited, India, with storage instructions and a QR code for medication guide access.*

FDA Label Image

100 mg (100s)

Quetiapine Tablets USP 100 mg oral tablets packaging label, containing 100 tablets. The label indicates quetiapine fumarate as the active ingredient equivalent to 100 mg quetiapine, manufactured by Lupin Pharmaceuticals, Inc., Baltimore, Maryland, USA, and Lupin Limited, India. Includes storage instructions, a barcode, and QR code for medication guide access.*

FDA Label Image

200 mg (100s)

Label for Quetiapine Tablets USP 200 mg, featuring 100 tablets in the package. The label includes the NDC 68180-448-01, manufacturer Lupin Pharmaceuticals, Inc., and provides storage, dosage, and warning information. A barcode and a QR code linking to the medication guide are also present.*

FDA Label Image

300 mg (100s)

Label for Quetiapine Tablets USP 300 mg by Lupin Pharmaceuticals, Inc. The oral tablet package contains 100 tablets. The label features dosage information, storage instructions, a barcode, a QR code for the medication guide, and manufacturer details including Lupin Limited in India.*

FDA Label Image

400 mg (100s)

Label for Quetiapine Tablets USP 400 mg by Lupin Pharmaceuticals, Inc. The label includes instructions to dispense the Medication Guide, states Rx only, and indicates a package size of 100 tablets. It notes each tablet contains 460.48 mg quetiapine fumarate USP equivalent to 400 mg quetiapine. Storage instructions, a barcode, manufacturer details, and a QR code for the Medication Guide are also present.*

* 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.