Fluoxetine Tablet, Film Coated
Product Images NDC 16714-112

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 16714-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Container1 (Container1)

Fluoxetine 10 mg film-coated tablets label from NorthStar Rx LLC. The label indicates the dosage strength, tablet count of 100, and highlights dispensing instructions. The product is identified as prescription only and includes storage and handling information. Manufacturer details for Dr. Reddy's Laboratories Limited in India are also visible, along with a barcode and National Drug Code (NDC) 16714-112-02.*

FDA Label Image

Container2 (Container2)

Label for Fluoxetine Tablets USP 20 mg film-coated tablets by NorthStar Rx LLC. The label states the product is for prescription use only, contains 100 tablets, and includes dosing and storage instructions. It also features the NDC 16714-113-02 and manufacturing information by Dr. Reddy's Laboratories Limited in India.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of Fluoxetine hydrochloride, showing its molecular arrangement with aromatic rings and substituents as visually represented in the image.*

* 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.