Fluoxetine Capsule
Product Images NDC 80425-0313

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 80425-0313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of 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

Description (Description)

Chemical structure diagram of Fluoxetine showing its molecular configuration including the trifluoromethyl-substituted phenyl group, ether linkage, and secondary amine hydrochloride.*

FDA Label Image

Label 1 (Fluoxetine HCl 20mg 80425 0313 01)

Fluoxetine HCL 20 mg capsule bottle label for 30 capsules, labeled by Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions (20-25°C), a barcode, and a comparison reference to Prozac. The lot number and expiration date (12/31/2025) are partially redacted.*

FDA Label Image

Label 2 (Fluoxetine HCl 20mg 80425 0313 02)

Fluoxetine HCl 20 mg capsule label from Advanced Rx Pharmacy of Tennessee, LLC, indicating a prescription product with a 60-capsule count. The label includes storage instructions (20-25°C), a barcode, NDC numbers, lot number, and expiration date of 12/31/2025. It compares the product to Prozac.*

FDA Label Image

Label 3 (Fluoxetine HCl 20mg 80425 0313 03)

Fluoxetine HCL 20 mg capsules packaging label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions at 20°-25°C (68°-77°F) and compares the product to Prozac. The label displays the NDC 80425-0313, lot number, expiration date 12/31/2025, and information for Sciegen Pharmac as the manufacturer.*

* 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.