Cymbalta
Product Images NDC 68151-4734

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Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Cymbalta (NDC 68151-4734). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carilion Materials Management, 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

Structural Formula (Cymbalta 01)

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Figure 3 (Cymbalta 02)

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Figure 4 (Cymbalta 03)

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Figure 5 (Cymbalta 13)

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Figure 6 (Cymbalta 14)

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Figure 7 (Cymbalta 15)

Figure 7 (Cymbalta 15)
The text describes a chart or graph that shows the percentage of improvement in pain from baseline in patients who received a placebo and those who received CYM60/120 mg once a day. The percentages range from 0% to 100%, with the highest percentage of improvement at 100% in the group receiving CYM60/120 mg once a day. The chart also shows different levels of percentage improvement in pain from baseline at different points on the graph.*
FDA Label Image

Figure 8 (Cymbalta 16)

Figure 8 (Cymbalta 16)
This appears to be a chart comparing the percentage of patients who have improved from baseline pain scores when taking either a placebo or CYMB0 mg once daily. The chart shows that 100% of patients improved when taking the CYMB0 mg once daily medication, represented by a solid line. The dotted line represents the improvement percentage for patients taking a placebo. The x-axis of the chart shows the levels of improvement in increments of 10%, and the y-axis represents the percentage of patients who have achieved that level of improvement.*
FDA Label Image

Figure 9 (Cymbalta 17)

Figure 9 (Cymbalta 17)
This text describes a graph or chart showing the percentage of patients who improved while taking a placebo versus CYM60/120 mg once daily. The chart also includes percentage improvement in pain from baseline.*
FDA Label Image

Figure 1 (Cymbalta 18)

Figure 1 (Cymbalta 18)
The graph shows the proportion of patients with relapse over time (in days) after randomization for a treatment group (CYMBALTA) and a placebo group. The X-axis represents the number of days, ranging from 0 to 250, and the Y-axis represents the proportion of patients with relapse, ranging from 0 to 1. The CYMBALTA treatment group has a lower proportion of patients with relapse compared to the placebo group.*
FDA Label Image

Figure 2 (Cymbalta 19)

FDA Label Image

Label Image (Lbl681514734)

Label Image (Lbl681514734)
This is a medication description for Cymbalta (generic name: Duloxetine) which is a 20mg delayed-release capsule produced by Lilly. The expiration date of the medication is 07/14 and the manufacturer's lot number is W010414SN20. It is a prescription-only drug with the code PDM: 4734.*

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