Duloxetine D/r Capsule, Delayed Release
Product Images NDC 72189-661

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Duloxetine D/r (NDC 72189-661). 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

72189-661-30 (72189 661 30)

Label for Duloxetine D/R 30 mg capsules, delayed release, with a package count of 30 capsules. The label indicates this product is generic for Cymbalta and is distributed by Direct_Rx. The label includes lot sample information with expiration date 4/30/2027 and manufacturing NDC codes visible.*

FDA Label Image

72189-661-60 (72189 661 60)

Label for Duloxetine D/R 30 mg delayed-release capsules, package of 60 capsules. It states the product is a generic form of Cymbalta, with each capsule containing 33.7 mg of duloxetine hydrochloride USP equivalent to 30 mg duloxetine. The label includes lot and expiration information and indicates packaging and distribution by Direct Rx.*

* 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.