Quetiapine Tablet, Extended Release
Product Images NDC 68001-602

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine (NDC 68001-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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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Chemical structure of Quetiapine fumarate, showing the molecular arrangement of quetiapine with the fumarate moiety, as used in the pharmaceutical formulation.*

FDA Label Image

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A Kaplan-Meier curve showing the proportion of patients with relapse (%) over time in months for two groups: PLA (placebo) and QTP XR (Quetiapine extended release). The graph compares relapse rates over a 7-month period, with PLA showing a higher relapse proportion than QTP XR.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse (%) over time (weeks). Two groups are compared: QTP+LIVAL and PLA+LIVAL, showing differing relapse rates across a 100-week period.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse (%) over time in weeks, comparing two groups labeled QTP+ LI/VAL and PLA+ LI/VAL. The graph shows the relapse proportion increasing over approximately 100 weeks for both groups, with PLA+ LI/VAL consistently higher than QTP+ LI/VAL.*

FDA Label Image

Quetiapine Er Tab 50mg (3ec5c4ad 8a55 4091 Ada4 4e009332a5ec 06)

Label for Quetiapine Extended-Release Tablets, USP 50 mg by BluePoint Laboratories. The label states the dosage form as extended-release tablets with 50 mg strength, containing 57.57 mg of Quetiapine Fumarate USP equivalent to 50 mg of Quetiapine. It includes storage instructions (20°C to 25°C), usual dosage (once daily), and manufacturer information: Unichem Laboratories Ltd., India. The package contains 60 tablets.*

FDA Label Image

Quetiapine Er Tabs 150mg (3ec5c4ad 8a55 4091 Ada4 4e009332a5ec 07)

Label for Quetiapine Extended-Release Tablets, USP 150 mg by BluePoint Laboratories. It is an oral tablet with 60 tablets per container. Manufactured by Unichem Laboratories Ltd., India. The label includes storage instructions, dosage guidance as once daily, and a warning to keep out of reach of children. NDC 68001-599-06.*

FDA Label Image

Quetiapine Er Tabs 200mg (3ec5c4ad 8a55 4091 Ada4 4e009332a5ec 08)

This label panel for Quetiapine Extended-Release Tablets, USP shows the 200 mg strength, with directions to swallow whole and not to split or chew. It includes storage instructions, a warning to keep out of children's reach, and advises pharmacists to provide the medication guide. The label indicates the manufacturer as UNICHEM LABORATORIES LTD. and the labeler as BluePoint Laboratories. The package contains 60 tablets.*

FDA Label Image

Quetiapine Er Tabs 300mg (3ec5c4ad 8a55 4091 Ada4 4e009332a5ec 09)

Label for Quetiapine Extended-Release Tablets, USP 300 mg, oral tablet, extended release form. The label includes dosage instructions, storage conditions, and warnings. It is manufactured by Unichem Laboratories Ltd. for BluePoint Laboratories. The package contains 60 tablets and is marked Rx Only with NDC 68001-601-06.*

FDA Label Image

Quetiapine Er Tabs 400mg (3ec5c4ad 8a55 4091 Ada4 4e009332a5ec 10)

Label for Quetiapine Extended-Release Tablets, USP 400 mg oral tablets by BluePoint Laboratories. The label states each extended-release tablet contains 460.52 mg Quetiapine Fumarate USP, equivalent to 400 mg Quetiapine, with instructions to swallow whole without splitting or crushing. The package contains 60 tablets and is manufactured by Unichem Laboratories Ltd in India.*

* 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.