Tamsulosin Hydrochloride Capsule
Product Images NDC 60760-598

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Tamsulosin Hydrochloride (NDC 60760-598). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary�s Medical Park Pharmacy, 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

Tamsulosin 60760 598 90

Tamsulosin 60760 598 90
This is a description of Tamsulosin Hydrochloride Capsules, USP 0.4mg. The bottle contains 90 capsules with the NDC code 60760-598-90, Lot number 222277?, and expiration date 72-77. The medication is manufactured by Aurobindo Pharma USA, located at East Windosor in NJ, made in India. The label also provides directions for use and storage temperature recommendations.*
FDA Label Image

Figure 1 Mean Plasma Tamsulosin Hydrochloride Concentrations Following Single-dose Administration Of Tamsulosin Hydrochloride Capsules 0.4 mg Under Fasted And Fed Conditions (n=8) (Tamsulosin Fig1)

Figure 1 Mean Plasma Tamsulosin Hydrochloride Concentrations Following Single-dose Administration Of Tamsulosin Hydrochloride Capsules 0.4 mg Under Fasted And Fed Conditions (n=8) (Tamsulosin Fig1)
This appears to be a figure with two graphs showing the mean plasma concentrations of tamsulosin hydrochloride capsules 0.4 mg under fasted and fed conditions. The x-axis shows time in hours, while the y-axis shows the concentration of the drug.*
FDA Label Image

Figure 2a Mean Change From Baseline In Total Aua Symptom Score (0 To 35) Study 1 (Tamsulosin Fig2)

Figure 2a Mean Change From Baseline In Total Aua Symptom Score (0 To 35) Study 1 (Tamsulosin Fig2)
This appears to be a figure (Figure 2A) displaying the mean change from baseline in Total AUA Symptom Score (measured on a scale of 0 to 35) in Study 1. The figure compares the results of the treatment (0.08mg) to a placebo over a duration of 13 weeks using LOCF analysis. The number of participants (n) in each group is provided. No further information is available from the given text.*
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Figure 2b Mean Change From Baseline In Total Aua Symptom Score (0 To 35) Study 2 (Tamsulosin Fig3)

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Figure 3a Mean Increase In Peak Urine Flow Rate (ml/sec) Study 1 (Tamsulosin Fig4)

Figure 3a Mean Increase In Peak Urine Flow Rate (ml/sec) Study 1 (Tamsulosin Fig4)
The figure 3A shows the mean increase in peak urine flow rate in L/sec for study 1. The treatment groups include 0.08mg, 0.4mg, and Placebo. The mean change in mL/sec is shown over the duration of treatment in weeks. There were different sample sizes for each group ranging from 621 to 755.*
FDA Label Image

Figure 3b Mean Increase In Peak Urine Flow Rate (ml/sec) Study 2 (Tamsulosin Fig5)

Figure 3b Mean Increase In Peak Urine Flow Rate (ml/sec) Study 2 (Tamsulosin Fig5)
This text appears to be a figure caption or title related to a study investigating the mean increase in peak urine flow rate. The figure shows the results of Study 2 and displays the change in flow rate (measured in mL/Sec) over the course of 20 weeks of treatment. There are also some unreadable characters present.*
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Chemical Structure (Tamsulosin Str)

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