Quetiapine Tablet, Film Coated
Product Images NDC 0904-6640

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine (NDC 0904-6640). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

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Label for Quetiapine tablets, USP 400 mg unit dose by Major Pharmaceuticals. The film-coated oral tablets are packaged as 100 tablets per unit dose. The label includes storage instructions, dosage caution to see product insert, and a warning to keep out of reach of children. The label shows NDC 0904-6643-61 and manufacturer and distributor information.*

FDA Label Image

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Packaging label for Quetiapine Tablets USP 300 mg by Major Pharmaceuticals. The label states the product as unit dose, with 100 tablets in the package. It includes directions for pharmacist dispensing with medication guide, prescription only (Rx only) status, storage instructions, and a warning to keep out of reach of children. The label shows the NDC 0904-6642-61 and manufacturing and distribution information.*

FDA Label Image

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Quetiapine 200 mg unit dose tablets, USP, oral film-coated tablets from Major Pharmaceuticals. The label indicates the strength as 200 mg per tablet, packaging contains 100 tablets. Includes storage instructions, dosage advisory to consult product insert, and a pharmacy dispensing note emphasizing the medication guide. Distributed by Major Pharmaceuticals with additional distributor information noted.*

FDA Label Image

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Quetiapine 100 mg unit dose tablets, USP label from Major Pharmaceuticals. The label includes dosing information, storage instructions, and warnings. It states the product is prescription only and contains 100 tablets. Manufactured by Alkem Laboratories Ltd. and distributed by Ascend Laboratories, LLC and Major Pharmaceuticals in Livonia, MI. The label features the Major Pharmaceuticals logo and a barcode.*

FDA Label Image

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Quetiapine 50 mg film-coated tablets unit dose label from Major Pharmaceuticals. The label shows the NDC number 09046-6639-61 and indicates the package contains 100 tablets. It includes storage instructions and a warning to keep out of reach of children. Manufacturer and distributor information is present along with barcode.*

FDA Label Image

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Quetiapine 25 mg film-coated tablets label from Major Pharmaceuticals. The label indicates the drug is for oral use, sold as a unit dose with 100 tablets per package. It includes dosage strength, dispensing instructions, and storage conditions, along with manufacturer and distributor details. The label features the Major Pharmaceuticals logo and barcode.*

FDA Label Image

Figure 1 (Quetiapine Fig1)

Kaplan-Meier curves showing the proportion of patients with relapse over time (weeks) in a study comparing QTP+LIV/VAL and PLA+LIV/VAL treatment groups. The graph plots relapse percentages on the Y-axis and time in weeks on the X-axis to depict time to recurrence of a mood event.*

FDA Label Image

Figure 2 (Quetiapine Fig2)

A Kaplan-Meier curve chart showing the time to recurrence of a mood event over 100 weeks. The y-axis represents the proportion of patients with relapse (%) from 0 to 100, and the x-axis indicates time in weeks from 0 to 100. Two lines compare QTP+ LIVAL versus PLA+ LIVAL treatment groups, with the PLA+ LIVAL line showing a higher proportion of relapse over time.*

FDA Label Image

Structure (Quetiapine Stru)

Chemical structure diagram of quetiapine fumarate depicting the molecular arrangement of quetiapine ion paired with fumarate ions, showing the components of this prescription drug's active ingredient.*

* 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.