Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 47335-907

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 Quetiapine Fumarate (NDC 47335-907). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

100 mg

100 mg
Label for Quetiapine Tablets, USP 100 mg, film-coated oral tablets, packaged as 100 tablets. The label indicates 'Rx only' and instructs pharmacists to dispense with a medication guide. It includes the NDC code 47335-904-88 and the Sun Pharmaceutical Industries, Inc. logo.*
FDA Label Image

200 mg

200 mg
Label for Quetiapine Tablets USP 200 mg, film-coated oral tablets by Sun Pharmaceutical Industries, Inc. The label states each tablet contains quetiapine fumarate equivalent to 200 mg quetiapine. It includes storage instructions, a warning to keep out of children's reach, and notes Rx-only with a count of 100 tablets. Manufacturer details in India are also visible.*
FDA Label Image

25mg (25mg)

25mg (25mg)
Label for Quetiapine Tablets USP 25 mg film-coated tablets by Sun Pharmaceutical Industries, Inc. The package contains 100 tablets. The label includes pharmacy dispensing instructions and a barcode with the NDC 47335-902-88.*
FDA Label Image

300 mg

300 mg
Quetiapine Tablets USP 300 mg film-coated tablets label from Sun Pharmaceutical Industries, Inc. The label indicates 100 tablets per package, with storage instructions and a warning to keep out of reach of children. Distributed by Sun Pharmaceutical Industries, Inc., manufactured by Sun Pharmaceutical Industries Ltd., India. Includes pharmacist dispensing instruction and Medication Guide notice.*
FDA Label Image

400 mg

400 mg
Label for Quetiapine Tablets USP 400 mg film-coated tablets by Sun Pharmaceutical Industries, Inc. The label shows storage instructions, a warning to keep out of reach of children, and notes 100 tablets per bottle. It includes a barcode and distributor and manufacturer details.*
FDA Label Image

50 mg

50 mg
Label for Quetiapine Tablets, USP 50 mg, film-coated oral tablets. The label indicates a package size of 100 tablets and includes a notice for pharmacists to dispense with a medication guide. The labeler is Sun Pharmaceutical Industries, Inc.*
FDA Label Image

Quetiapine-fig-1 (Quetiapine Fig 1)

Quetiapine-fig-1 (Quetiapine Fig 1)
A Kaplan-Meier curve graph titled 'Kaplan-Meier Curves of Time to Recurrence of a Mood Event (Study 7)' showing the proportion of patients with relapse (%) over time in weeks. Two curves represent treatment groups: QTP + LI/VAL (dashed line) and PLA + LI/VAL (solid line), with the QTP group showing a lower relapse proportion over time compared to the PLA group.*
FDA Label Image

Quetiapine-fig-2 (Quetiapine Fig 2)

Quetiapine-fig-2 (Quetiapine Fig 2)
Kaplan-Meier curves depicting the proportion of patients with relapse over time in weeks for a mood event from Study 8. The graph compares two groups: QTP+LI/VAL and PLA+LI/VAL, showing relapse percentages on the Y-axis and time in weeks on the X-axis, with QTP+LI/VAL group showing a lower proportion of relapse over time compared to PLA+LI/VAL.*
FDA Label Image

Quetiapine-structure (Quetiapine Structure)

Quetiapine-structure (Quetiapine Structure)
Chemical structure of quetiapine fumarate, showing the molecular arrangement including the quetiapine moiety and fumarate ions.*

* 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.