Quetiapine Fumarate Tablet
Product Images NDC 71610-136

9 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · 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 71610-136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Bottle Label 300 mg (71610 0127 18)

Bottle Label 300 mg (71610 0127 18)
Label for Quetiapine 300 mg oral tablets, containing 3000 tablets per package. The label includes the NDC number 71610-0127-18 and notes that this product is repackaged by Aphena Pharma Solutions - Tennessee, LLC, with original manufacturing by West-Ward Pharmaceuticals Corp., Columbus, OH. The label indicates RX only use and provides storage instructions and lot and expiration information.*
FDA Label Image

Bottle Label 200 mg (71610 0128 15)

Bottle Label 200 mg (71610 0128 15)
Label for Quetiapine 200 mg oral tablets, containing 15 tablets. The label includes storage instructions and indicates repackaging by Aphena Pharma Solutions - Tennessee, LLC. The original manufacturer noted is West-Ward Pharmaceuticals Corp., Columbus, OH. The label bears the NDC number 71610-0128-15 and states the product is RX only.*
FDA Label Image

Bottle Label 100 mg (71610 0136 15)

Bottle Label 100 mg (71610 0136 15)
Label for Quetiapine 100 mg oral tablets, containing 15 tablets per package. The label shows storage instructions, manufacturer West-Ward Pharmaceuticals Corp. from Columbus, OH, and repackager Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN. It includes the NDC number 71610-0136-15 and indicates RX Only.*
FDA Label Image

Bottle Label 25 mg (71610 0140 30)

Bottle Label 25 mg (71610 0140 30)
Label for Quetiapine 25 mg tablets, containing 30 tablets in the package. The product is labeled for oral use and manufactured by West-Ward Pharmaceuticals Corp., Columbus, OH, and repackaged by Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN. The label includes storage instructions, lot number, expiration date, and NDC 71610-0140-30.*
FDA Label Image

Bottle Label 400 mg (71610 0141 18)

Bottle Label 400 mg (71610 0141 18)
Label for Quetiapine 400 mg oral tablets, with a total count of 3000 tablets. The label includes storage instructions, manufacturer information (West-Ward Pharmaceuticals Corp., Columbus, OH), and repackaging details by Aphena Pharma Solutions - Tennessee, LLC. The label also indicates prescription use only and includes batch and lot numbers along with bar codes.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chem.jpg (Chem)

Chem.jpg (Chem)
Chemical structure of the active ingredient Quetiapine Fumarate, showing the molecular arrangement of Quetiapine and fumarate components.*
FDA Label Image

Fig1.jpg (Fig1)

Fig1.jpg (Fig1)
A Kaplan-Meier survival curve chart depicting the proportion of patients with relapse (%) over time in weeks. Two groups are compared: a dashed line represents QTP+LI/VAL and a solid line represents PLA+LI/VAL, showing differences in relapse proportions across a 100-week period.*
FDA Label Image

Fig2.jpg (Fig2)

Fig2.jpg (Fig2)
A Kaplan-Meier survival curve chart showing the proportion of patients with relapse (%) over time (weeks) for two treatment groups: Quetiapine (QTP) with Lithium/Valproate (LI/VAL) and Placebo (PLA) with Lithium/Valproate (LI/VAL). The chart plots relapse proportion on the Y-axis from 0 to 100% and time on the X-axis from 0 to 100 weeks, with the QTP+LI/VAL group as a dashed line and the PLA+LI/VAL group as a solid line.*

* 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.