Fluoxetine Tablet, Film Coated
Product Images NDC 59651-308

3 FDA label images from Aurobindo Pharma Limited · 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 59651-308). 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 Limited. The label includes dosage information, storage instructions at 20° to 25°C, child safety warnings, and pharmacist guidance. The package contains 30 tablets. The product is distributed by Aurobindo Pharma USA, Inc., made in India, with a printed NDC of 59651-308-30 and a barcode on the right side.*
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 by Aurobindo Pharma Limited. The label states each tablet contains fluoxetine hydrochloride USP equivalent to 20 mg fluoxetine. Packaging includes 30 tablets and provides storage conditions and distribution information for Aurobindo Pharma USA, Inc.*
FDA Label Image

Chemical Structure (Fluoxetine Str)

Chemical Structure (Fluoxetine Str)
Chemical structure of Fluoxetine hydrochloride, depicting the molecular arrangement of atoms including a fluorophenyl group attached to an ether and amine side chain with a phenyl ring, along with hydrochloride (HCl).*

* 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.