Fluoxetine Solution
Product Images NDC 0121-0721

3 FDA label images from Pai Holdings, Llc Dba Pai Pharma · 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 0121-0721). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Chemical Structure (Fluoxetine 01)

Chemical Structure (Fluoxetine 01)
Chemical structure diagram of Fluoxetine hydrochloride, showing its molecular components including a trifluoromethyl group attached to a benzene ring, an ether linkage, and an amine group with a hydrochloride salt.*
FDA Label Image

Principal Display Panel (120 mL Bottle Label)

Principal Display Panel (120 mL Bottle Label)
Fluoxetine Oral Solution USP 20 mg/5 mL label shows the product name, strength, and dosage form clearly. It indicates the volume as 120 mL and includes directions for pharmacists to provide a medication guide. The label specifies storage instructions and the labeler, PAI Pharmaceutical Associates, Inc., Greenville, SC.*
FDA Label Image

Principal Display Panel (5 mL Cup Label)

Principal Display Panel (5 mL Cup Label)
Label for Fluoxetine Oral Solution USP, 20 mg per 5 mL, delivering 5 mL per dose. The label includes the National Drug Code (NDC) 0121-4721-05 and states the product is Rx only and not child-resistant. Manufacturer information lists Pharmaceutical Associates, Inc., Greenville, SC.*

* 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.