Fluoxetine Hydrochloride Capsule, Delayed Release Pellets
Product Images NDC 55111-284

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fluoxetine Hydrochloride (NDC 55111-284). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories 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

Carton (Carton)

Packaging label for Fluoxetine Delayed-Release Capsules, USP 90 mg, once-weekly, prescription oral capsules by Dr. Reddy's Laboratories Limited. The unit of use pack contains 4 capsules (1 x 4 unit-dose). The label includes instructions for blister opening and dispensing guidance for pharmacists, with barcode and manufacturer details.*

FDA Label Image

Structure (Structure)

Chemical structure of fluoxetine hydrochloride, depicting its molecular framework including aromatic rings and functional groups consistent with the active ingredient fluoxetine hydrochloride.*

* 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.