Fluoxetine
Product Images NDC 61919-869

3 FDA label images from Direct Rx · 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 61919-869). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

61919 869 30

61919 869 30
Fluoxetine 20 mg capsule label from DIRECT RX. The label shows 30 capsules in the package. It mentions Fluoxetine hydrochloride USP equivalent to 20 mg of fluoxetine and notes it is a generic for Prozac. The label includes NDC 61919-869, lot number, expiration date, manufacturing and packaging information, and storage instructions.*
FDA Label Image

61919 869 60

61919 869 60
FLUOXETINE 20 mg capsules, bottle label showing 60 capsules in the package. Product is generic for Prozac, each capsule contains fluoxetine hydrochloride USP equivalent to 20 mg fluoxetine. Label indicates packaging and distribution by DIRECT RX along with lot number 305E2110 and expiration date 2/29/24.*
FDA Label Image

869 (869 90)

869 (869 90)
FLUOXETINE 20mg 90 Caps label by DIRECT RX. The label indicates the product is a generic for PROZAC, fluoxetine hydrochloride capsules, equivalent to 20mg fluoxetine base. The label includes warnings for alcohol use and overdose symptoms, manufacturer Aurboidno Pharma USA, Inc., and a lot number with expiration date 10/18/2016.*

* 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.