Duloxetine
Product Images NDC 67046-679

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Duloxetine (NDC 67046-679). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Contract Pharmacy Services-pa, 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

D3 (Duloxetine 30mg 691)

D3 (Duloxetine 30mg 691)
DULOXETINE DR is a medication that comes in a bottle containing 30 capsules, each capsule has a dosage of 30mg. The lot number is not provided, but the expiry date is 12/31/2020. This medication is sold only on a doctor's prescription. The manufacturer is Breckenridge and the standard global trade identification number is GTINDD387046891302. The pill ID is B747. Please refer to the accompanying literature for dosage. The medication should be stored at a temperature range of 15-30°C (50-85°F). Each capsule contains 33.7mg of duloxetine hydrochloride USP equivalent to 30mg duloxetine. The medication is packaged by Contract Pharmacy Services in Pennsylvania and the National Drug Code (NDC) is 67045-391-30.*
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D6 (Duloxetine 60mg 679)

D6 (Duloxetine 60mg 679)
This is a medication called Duloxetine available in the form of capsules with 60mg strength in a pack of 30. The medicine should be stored at a temperature between 15-30°C (58-86°F). It contains Duloxetine Hydrochloride USP equivalent to 67.3mg. For dosage information, you can refer to the accompanying literature. It is an RX-only medicine that can be purchased with a proper prescription. The information contains the Lot, pill ID, Sin, GTIN, and other details. Expiration details can be found in the text.*
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Chemical Structure (Duloxetine 01)

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Figure 1 (Duloxetine 02)

Figure 1 (Duloxetine 02)
The text represents a graph showing the proportion of patients who had a relapse based on the treatment they received (placebo or duloxetine) and the time (in days) from randomization to relapse.*
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Figure 2 (Duloxetine 03)

Figure 2 (Duloxetine 03)
The given text represents a chart showing the proportion of patients who experienced relapse over the course of time after being randomized to either Placebo or Duloxetine treatment. It shows the proportion of patients experiencing relapse decreasing over time in both treatment groups, with Duloxetine showing a lower proportion of relapses compared to Placebo.*
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Figure 3 (Duloxetine 04)

Figure 3 (Duloxetine 04)
This appears to be a graph or chart showing the percentage of patients who improved and the percentage of improvement in pain from baseline. Without more context or labels it is difficult to provide a more specific description.*
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Figure 4 (Duloxetine 05)

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Figure 7 (Duloxetine 06)

Figure 7 (Duloxetine 06)
The text shows a chart of the percentage of patients improved with a placebo and Duloxetine at varying doses. It also includes a graph measuring the percent improvement in pain from baseline.*
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Figure 8 (Duloxetine 07)

Figure 8 (Duloxetine 07)
This is a graph displaying the percentage of patients' improvement in pain from baseline (BOCF) after taking a placebo or DUL 60 mg once daily medication. The improvement rates are shown on the y-axis and range from 0% to 100%. The x-axis shows the different treatment options. It appears that the DUL 60 mg once daily medication resulted in a higher rate of improvement compared to the placebo, with a 100% improvement rate noted.*
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Figure 9 (Duloxetine 08)

Figure 9 (Duloxetine 08)
The text presents a chart comparing the percentage of patients improved in pain from baseline for a placebo group and a group taking DUL 60/120 mg once daily. The chart also includes a graph illustrating the percent improvement in pain from baseline (BOCF) for the different treatment groups.*

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