Duloxetine Capsule, Delayed Release Pellets
Product Images NDC 68001-368

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Duloxetine (NDC 68001-368). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Duloxetine 01)

Chemical Structure (Duloxetine 01)
FDA Label Image

Figure 1 (Duloxetine 02)

Figure 1 (Duloxetine 02)
FDA Label Image

Figure 2 (Duloxetine 03)

Figure 2 (Duloxetine 03)
FDA Label Image

Figure 3 (Duloxetine 04)

Figure 3 (Duloxetine 04)
FDA Label Image

Figure 4 (Duloxetine 05)

Figure 4 (Duloxetine 05)
FDA Label Image

Figure 7 (Duloxetine 06)

Figure 7 (Duloxetine 06)
FDA Label Image

Figure 8 (Duloxetine 07)

Figure 8 (Duloxetine 07)
FDA Label Image

Figure 9 (Duloxetine 08)

Figure 9 (Duloxetine 08)
FDA Label Image

Duloxetine 09

Duloxetine 09
This appears to be a chart or table showing the percentage of patients who experienced improvements in pain, with values ranging from 0 to 280. Without additional context or information, it is unclear what the units or specific measurements represent.*
FDA Label Image

Duloxetine 10

Duloxetine 10
FDA Label Image

Duloxetine 14

Duloxetine 14
This text contains medication information for Duloxetine Delayed-Release Capsules, USP. Each capsule contains 49 E-ispense and must be kept in a tightly closed container. The medication is manufactured by TOWA Pharmaceutical Europe, S.L. and is RxOnly, therefore it must be dispensed by a pharmacist. It is important to keep the medication out of reach of children and store it at 25°C (77°F). The text also includes the NDC code (68001-368-04) and an expiration date (022021). The rest of the text seems to be a mix of characters without any clear meaning.*

* 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.