Sildenafil Tablet, Film Coated
Product Images NDC 82647-210
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Sildenafil (NDC 82647-210). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Reyoung Corporation, 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
100mg-30s.jpg (100mg 30s)
25mg-1000s.jpg (25mg 1000s)
25mg-30s.jpg (25mg 30s)
50mg-1000s.jpg (50mg 1000s)
50mg-30s.jpg (50mg 30s)
Figure1.jpg (Figure1)
Figure2.jpg (Figure2)
Figure3.jpg (Figure3)
Figure4.jpg (Figure4)
Figure5.jpg (Figure5)
Figure6.jpg (Figure6)
Figure7.jpg (Figure7)
Structure.jpg (Structure)
Table-2.jpg (Table 2)
Table 2 shows the adverse reactions reported by more than 2% of patients treated with Sildenafil in flexible-dose phase II/III studies. These reactions were more frequent than those reported with the placebo. The adverse reactions reported include headache, flushing, dyspepsia, nasal congestion, abnormal vision, back pain, dizziness, and rash. Abnormal vision was predominantly mild and transient, with a color tinge to vision, and only one patient discontinued the treatment due to abnormal vision.*
Tablet-3 (Table 3)
The table presents hemodynamic data in patients with stable ischemic heart disease before and after the intravenous administration of 40 mg of Sildenafil. The data includes mean values and standard deviation for PAOP, PAP, RAP, SAP, diastolic SAP, cardiac output, and heart rate. The data is presented before and 4 minutes after exercise, with the patients being divided into two groups, one receiving Sildenafil and one not.*
Table1.jpg (Table1)
Table 1 shows the adverse reactions reported by patients treated with sildenafil in fixed-dose Phase I/III studies. The table includes the percentage of patients experiencing adverse reactions, categorized by dosage. Adverse reactions that were reported by more than 2% of patients and were more frequent than placebo are presented. The adverse reactions listed include headache, flushing, dyspepsia, abnormal vision, nasal congestion, back pain, myalgia, nausea, dizziness, and rash. Abnormal vision was described as mild to moderate in severity and transient, with a predominantly color tinge to vision, but also increased sensitivity to light or blurred vision.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.