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)

The text consists of information about a medication named Duloxetine D/R 30mg, with details such as NDC number, lot number, expiration date, and manufacturer information. It mentions that each capsule contains 30mg of Duloxetine Hydrochloride USP and that it is a generic for Cymbalta. The medication is distributed by Ajanta Pharma USA Inc. The dosage instructions are mentioned to refer to the package. The lot number and expiration date provided are associated with the samples. The text also includes details about the distribution and directions for use.*

FDA Label Image

72189-661-60 (72189 661 60)

This document seems to be a prescription label for the medication Duloxetine D/R 30mg, with information such as NDC codes, capsule count, lot number, expiration date, and dosage details. It includes important instructions on storage, dosage, caution, and the prescription being for the intended patient only. This prescription label mentions the generic equivalent for Cymbalta (CVmhalta) and is intended for use until the specified expiration date.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.