Tadalafil Tablet, Film Coated
Product Images NDC 69238-1349
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Product Visual Gallery
This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Tadalafil (NDC 69238-1349). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals Ny Llc, 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
2.5 mg (Tadalafil Tablets Usp 10)
This is a description of Tadalafil Tablets, USP with NDC code 69238-1346-3 for once-daily use. Each film-coated tablet contains 2.5mg of Tadalafil, USP. Dosage should not be split and an entire dose should be taken. It is Rx only and should be stored at 20° to 25°C (68° to 77°F) in a tight container. The tablets are manufactured by Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, INDIA and distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. It is important to keep this and all medications out of reach of children. There seems to be additional text that is unreadable due to error.*
5 mg (Tadalafil Tablets Usp 11)
This is a description of Tadalafil tablets with a concentration of 5mg per tablet. The recommended dose is provided in the accompanying literature, and the tablets should not be split. The drug should be stored between 20° to 25°C (68° to 77°F). The tablets are manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC.*
10 mg (Tadalafil Tablets Usp 12)
This is a description of Tadalafil tablets manufactured and distributed by Amneal Pharmaceuticals. It includes details on the quantity, dosage, and storage requirements of the tablets. The tablets should not be split, and the entire dose should be taken as prescribed. The tablets contain 10 mg of Tadalafil, and the usual dosage is provided in accompanying literature. The tablets should be kept in a tight container and stored at 20° to 25°C. The text also mentions the manufacturer's location and license number.*
20 mg (Tadalafil Tablets Usp 13)
This is a prescription medication with the National Drug Code 69238-1349-3. The medication is Tadalafil and it comes in the form of film-coated tablets of 20mg. The tablets should not be split, and the entire dose should be taken. The usual dosage should be according to the accompanying literature. It should be stored at 20° to 25°C (68° to 77°F), and this medication should be kept in a tight container and out of the reach of children. It is manufactured by Amneal Pharmaceuticals Pvt. Ltd. and Distributed by Amneal Pharmaceuticals LLC. It's an oral solid dosage unit, and the manufacturing license number is G/26/2137 Rev. 01-2019-00. However, there is a Non-Varnish Area for Lot and Exp. Dates measuring 26 x 28 mm, and it is not advisable to use this area for any treatment purpose.*
10 (Tadalafil Tablets Usp 2)
This appears to be a table or graph displaying the difference in blood pressure between a medication called Tadalafil and a placebo. The table shows standing and supine systolic and diastolic blood pressure readings. However, the table is not very legible and some characters are not recognizable, making it difficult to interpret the data.*
10 (Tadalafil Tablets Usp 3)
10 (Tadalafil Tablets Usp 4)
This is a study comparing the effects of different treatments (tadalafil, doxazosin, placebo) on systolic blood pressure. Information on dosages and administration times is provided. However, the output contains several errors and incomplete words, making it difficult to fully understand the study design.*
10 (Tadalafil Tablets Usp 5)
This is a chart showing the plasma concentration of Tadalafil in mcg/L at different time points after a single dose of 20 mg or 5 mg of Tadalafil, as well as once-daily 5 mg Tadalafil after 5 consecutive days of administration. The concentration reaches its peak at around 2 hours after administration and starts to decline gradually. Data is shown up to 120 hours (5 days) after the first dose.*
10 (Tadalafil Tablets Usp 6)
10 (Tadalafil Tablets Usp 7)
The text shows a comparison study between Tadalafil 5 mg and a placebo medication. The effectiveness of Tadalafil is denoted by a significant difference in the IPSS Total Score compared to the placebo medication. The duration of the treatment is also mentioned, but further details or conclusions cannot be made with this limited information.*
10 (Tadalafil Tablets Usp 8)
10 (Tadalafil Tablets Usp 9)
The text describes a comparison between Tadalafil 5mg and Placebo in relation to the change from the baseline in IPSS total score. It also states that the statistical analysis resulted in a significant difference between the two groups (p<0.01). However, no information is provided about the study design, objectives or outcomes other than the duration of treatment in weeks.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.