Fluoxetine Tablet, Film Coated
Product Images NDC 84386-104

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 84386-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (10 mg (30 Tablets Bottle))

Package Label-principal Display Panel (10 mg (30 Tablets Bottle))
Label for Fluoxetine Tablets, USP 10 mg film-coated tablets by Aurobindo Pharma USA, Inc. The label includes the NDC 84386-104-30, directions for storage (20° to 25°C), and instructions to keep the medication out of reach of children. The package contains 30 tablets and is marked Rx only. The label states that the product is made in India and includes a barcode.*
FDA Label Image

Package Label-principal Display Panel (20 mg (30 Tablets Bottle))

Package Label-principal Display Panel (20 mg (30 Tablets Bottle))
Label for Fluoxetine Tablets, USP 20 mg film-coated tablets, packaged with 30 tablets. The label states the active ingredient strength as 20 mg and includes handling instructions such as storage temperature and light protection. Distributed by Aurobindo Pharma USA, Inc., made in India, with a barcode and NDC 84386-105-30 visible.*
FDA Label Image

Chemical Structure (Fluoxetine Str)

Chemical Structure (Fluoxetine Str)
Chemical structure of Fluoxetine hydrochloride showing the molecular arrangement including a trifluoromethyl group, aromatic rings, and an amine side chain.*

* 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.