Finasteride Tablet, Film Coated
Product Images NDC 60687-428
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 Finasteride (NDC 60687-428). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by American Health Packaging, 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
50 Ud Carton
This is a description of the drug Finasteride, which is available in a 50 tablet pack for Rx-only use. The drug should not be used by women or children, and women who may be pregnant should avoid using it. Each film-coated tablet contains 0.97mg of the active ingredient. The suggested dosage for adults is 1 to 5 mg per day. The drug should be stored between 20°C to 25°C and protected from heat. The drug product is manufactured and distributed by Aurobindo Pharma USA Inc., and the packaging is done by Richmond & Packaging Inc.*
Ahp 428 01 65
Blister
Figure 1
Figure 2
This appears to be a part of a research study that includes a graph (Figure 2) indicating the percentage of patients, who underwent surgery for BPH, over a period of observation time (in months) in two groups - those who received Finasteride and those who received a placebo. The graph shows that the percentage of patients who had surgery for BPH in the Finasteride group was lower than the percentage in the placebo group. The text also includes some numerical data related to the number of events and the number of patients at risk in both the groups.*
Figure 3
This is a graph showing the percentages of patients who developed acute urinary retention over a period of 24 months. Two groups are being compared - placebo group and Finasteride group. At the end of 24 months, 16% of patients in the placebo group developed acute urinary retention while only 2% of patients in the Finasteride group developed it. The graph also shows the number of patients at risk over time and the number of events (urinary retention) that occurred at different time points.*
Figure 4
Figure 5
Structure
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.