Fluoxetine Tablet
Product Images NDC 64380-903

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 64380-903). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science 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

Fluoxetine Structural Formula (21c48549 64d1 480e 8e74 Fde61d6110b5 01)

Fluoxetine Structural Formula (21c48549 64d1 480e 8e74 Fde61d6110b5 01)
Chemical structure of fluoxetine, showing its molecular components including trifluoromethyl-substituted phenyl ring, ether linkage, and methylamine hydrochloride group.*
FDA Label Image

Fluoxetine Tablets 10 mg (30s)

Fluoxetine Tablets 10 mg (30s)
Label for Fluoxetine Tablets USP 10 mg by Strides Pharma Science Limited. The film-coated tablets each contain fluoxetine hydrochloride equivalent to 10 mg fluoxetine. The label includes storage instructions, a warning to keep medication out of reach of children, and specifies a package size of 30 tablets. Barcode and manufacturing/distributing details for Strides Pharma Science Limited are also present.*
FDA Label Image

Fluoxetine Tablets 20 mg (30s)

Fluoxetine Tablets 20 mg (30s)
Fluoxetine Tablets USP 20 mg label for oral tablets, manufactured by Strides Pharma Science Limited. The label indicates a package containing 30 tablets and includes storage instructions, dosage guidance reference, and safety warnings to keep out of reach of children. The label also features a barcode and distribution information for Strides Pharma Inc.*

* 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.