Fluoxetine Hydrochloride
Product Images NDC 53808-0988

3 FDA label images from State Of Florida Doh Central Pharmacy · 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 Hydrochloride (NDC 53808-0988). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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 Hydrochloride Chemical Structure (9f2aa395 87d1 4f3c 82de 26bbbe72f51d 01)

Fluoxetine Hydrochloride Chemical Structure (9f2aa395 87d1 4f3c 82de 26bbbe72f51d 01)
Chemical structure of Fluoxetine Hydrochloride showing its molecular formula C17H18F3NO•HCl and molecular weight 345.79.*
FDA Label Image

Fluoxetine 10 mg Label (Fluoxetine 10mg(aurobindo))

Fluoxetine 10 mg Label (Fluoxetine 10mg(aurobindo))
Label for Fluoxetine 10 mg capsules in a quantity of 30, marked RX only. The label indicates packaging by DOH Central Pharmacy in Tallahassee, FL, and lists a lot number and expiration date. A barcode and UPC number are also visible.*
FDA Label Image

Fluoxetine 20 mg Label (Fluoxetine 20mg(aurobindo))

Fluoxetine 20 mg Label (Fluoxetine 20mg(aurobindo))
Fluoxetine 20 mg capsules packaging label showing quantity of 30 capsules. The label includes manufacturer information as Aurobindo with packaging by Florida DOH Central Pharmacy, Tallahassee, FL. The label also displays a lot number and an expiration date, with a barcode and UPC code visible.*

* 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.