Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 46708-136

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 46708-136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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

100 mg 30's Bottle Pack (Quetiapine 100mg)

Quetiapine Fumarate Tablets 100 mg film-coated tablets label from Alembic Pharmaceuticals Limited. The label includes NDC 46708-136-30, quantity of 30 tablets, and warnings to keep out of reach of children. It instructs pharmacists to dispense the enclosed medication guide to each patient. Manufacturer address in Gujarat, India, is also visible.*

FDA Label Image

200 mg 30's Bottle Pack (Quetiapine 200mg)

Quetiapine Fumarate Tablets 200 mg film-coated oral tablets label from Alembic Pharmaceuticals Limited. The label indicates a package of 30 tablets, prescription only, with storage instructions and medication guide dispensing information. The NDC number 46708-137-30 is shown along with manufacturer details in Gujarat, India.*

FDA Label Image

25 mg 30's Bottle Pack (Quetiapine 25mg)

Label for Quetiapine Fumarate Tablets 25 mg, film-coated oral tablets, manufactured by Alembic Pharmaceuticals Limited. The label includes dosage strength, a barcode, packaging quantity of 30 tablets, and usage warnings including storage instructions and child safety.*

FDA Label Image

300 mg 30's Bottle Pack (Quetiapine 300mg)

Quetiapine Fumarate Tablets 300 mg film-coated oral tablets label from Alembic Pharmaceuticals Limited. The label includes the NDC 46708-138-30, packaging for 30 tablets, barcode, and storage instructions. It highlights the active ingredient strength and dispensing guidance for pharmacists.*

FDA Label Image

400 mg 30's Bottle Pack (Quetiapine 400mg)

Quetiapine Fumarate 400 mg film-coated tablets label from Alembic Pharmaceuticals Limited. The label shows the NDC number 46708-139-30, quantity of 30 tablets, and includes storage instructions and warnings. The label is primarily white with a pink border and features the Alembic logo in blue and green.*

FDA Label Image

50 mg 30's Bottle Pack (Quetiapine 50mg)

Quetiapine Fumarate Tablets 50 mg film-coated oral tablets packaging label. Contains 30 tablets per container. Label includes manufacturer Alembic Pharmaceuticals Limited and dosage instructions, with warning to keep out of reach of children. The label also displays the NDC 46708-135-30 and directions for pharmacists to dispense the Medication Guide to patients.*

FDA Label Image

Figure 1 (Quetiapine Fig1)

A Kaplan-Meier curve chart illustrating the time to recurrence of a mood event over weeks. The y-axis represents the proportion of patients with relapse in percentage, and the x-axis represents time in weeks. Two survival curves are shown, labeled as "QTZ LIVAL" and "PBO LIVAL," indicating comparative relapse rates over the study period.*

FDA Label Image

Figure 2 (Quetiapine Fig2)

A line graph showing the proportion of patients with relapse over a 100-week period. The x-axis represents time in weeks, and the y-axis indicates the proportion of patients (%) with relapse. Two lines compare QTP+LIVAL and PLA+LIVAL treatments, with QTP+LIVAL showing a higher relapse proportion over time.*

FDA Label Image

Structure (Quetiapine Str)

Chemical structure of quetiapine fumarate, showing the molecular arrangement of quetiapine along with the fumarate component. The diagram displays the two-part structure typical of this molecule.*

* 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.