Fluoxetine Hydrochloride Tablet, Film Coated
Product Images NDC 51672-5306

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluoxetine Hydrochloride (NDC 51672-5306). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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 01

Chemical structure of fluoxetine hydrochloride, illustrating its molecular arrangement including aromatic rings, trifluoromethyl group, and hydrochloride salt.*

FDA Label Image

Fluoxetine 02

Label for FLUOXETINE HYDROCHLORIDE 60 mg film-coated tablets, oral use. The label indicates a package of 30 tablets with NDC 51672-5306-6. It includes storage instructions to keep at 20° to 25°C and to protect from light. Distributed by Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY. The label notes it is a prescription drug (Rx only).*

FDA Label Image

Fluoxetine 03

Fluoxetine Tablets, USP 60 mg film-coated tablets packaging label showing a 500 tablet count. The label includes NDC 51672-5306-2 and states the drug is distributed by Taro Pharmaceuticals U.S.A., Inc. It also notes to dispense the medication guide to patients and contains storage and dosage instructions.*

* 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.