Quetiapine Fumarate Tablet
Product Images NDC 51407-071

9 FDA label images from Golden State Medical Supply, Inc. · 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 51407-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407 066 10lb

51407 066 10lb
Label for Quetiapine tablets, USP, 25 mg strength, package contains 1,000 tablets. The label displays the NDC number 51407-066-10 and indicates storage at 20° to 25°C. It is marked for prescription use only (Rx only) and mentions Golden State Medical Supply, Inc. as the labeler.*
FDA Label Image

51407 067 01lb

51407 067 01lb
Label for Quetiapine tablets, USP, 50 mg strength with 100 tablets per bottle. The label includes the NDC 51407-067-01 and states the product is Rx only. The labeler is shown as GSMS Incorporated, and storage instructions specify 20° to 25°C (68° to 77°F). Manufacturer details and barcode are also visible.*
FDA Label Image

51407 068 10lb

51407 068 10lb
Quetiapine Fumarate 100 mg tablets label by Golden State Medical Supply, Inc., showing the NDC 51407-068-10. The label indicates a package containing 1,000 tablets, with storage instructions at 20° to 25°C (68° to 77°F). The label features a barcode, lot, expiration, and serial number fields, and a notice to see the package insert for dosage information. Marked as prescription only (Rx only).*
FDA Label Image

51407 069 05lb

51407 069 05lb
Quetiapine Fumarate 200 mg tablets label by Golden State Medical Supply, Inc. The label shows the product name, strength as 200 mg, and a package size of 500 tablets. It includes the NDC number 51407-069-05 and indicates the product is for prescription use only. Storage instructions state to keep at 20° to 25°C (68° to 77°F). Additional details mention to see the package insert for dosage information.*
FDA Label Image

51407 070 05lb

51407 070 05lb
Label for Quetiapine Fumarate tablets, USP 300 mg strength, containing 500 tablets. The label includes the NDC number 51407-070-05, indicates the product is Rx only, and provides storage instructions at 20° to 25°C. The labeler is Golden State Medical Supply, Inc., manufactured by West-Ward Pharmaceuticals Corp. in Camarillo, CA.*
FDA Label Image

51407 071 01lb

51407 071 01lb
Label for Quetiapine Fumarate 400 mg oral tablets, USP, containing 100 tablets. The label shows the drug name in orange and black text, the NDC number 51407-071-01, and states "Rx only." The product is manufactured by Golden State Medical Supply, Inc. Storage instructions specify 20° to 25°C (68° to 77°F) controlled room temperature.*
FDA Label Image

Chem.jpg (Chem)

Chem.jpg (Chem)
Chemical structure of Quetiapine Fumarate, showing the molecular arrangement of the quetiapine moiety complexed with fumarate as part of this oral tablet product by Golden State Medical Supply, Inc.*
FDA Label Image

Fig1.jpg (Fig1)

Fig1.jpg (Fig1)
A line graph depicting the proportion of patients with relapse (%) over time (weeks). The graph includes two lines: a dashed line labeled QTP+LI/VAL and a solid line labeled PLA+LI/VAL, showing different relapse rates across approximately 100 weeks.*
FDA Label Image

Fig2.jpg (Fig2)

Fig2.jpg (Fig2)
A Kaplan-Meier survival curve showing the proportion of patients with relapse (%) over time in weeks. The graph compares two groups: QTP+LI/VAL represented by a dashed line, and PLA+LI/VAL represented by a solid line. The chart illustrates the increasing relapse rates over the course of approximately 100 weeks for each group.*

* 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.