Tadalafil Tablet, Film Coated
Product Images NDC 68071-3777

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Tadalafil (NDC 68071-3777). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,inc., 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

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This text provides a medication schedule comparison between 20mg tadalafil and 8g ad vonazosh at 08:00, and placebo. There is a regimen for 20mg tadalafil and 8g dose at 20:00, along with Placebo and 8g qd dorazosi at 18:00. The text also mentions a time after administration of tadalafil or placebo.*

FDA Label Image

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This text provides information on plasma Tadalafil concentrations (ug/L) over time following different dosages: a single 20mg dose, a single 5mg dose, and a once-daily 5mg dose for 5 consecutive days. Time intervals are shown in hours for the measurements.*

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This text appears to be a description of a pharmaceutical product containing Tadalafil 20mg. It provides information such as lot number, NDC numbers, expiration date, and a warning to keep the product out of reach of children and store at a controlled temperature of 68-77°F. It also advises contacting a doctor for medical advice about potential side effects and includes a reference to report side effects to the FDA.*

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