Tadalafil Tablet
Product Images NDC 82009-079

This is a description of a medication called Tadalafil. Each film-coated tablet contains 20 mg of Tadalafil. The tablets also contain FD&C yellow No 5 (Tartrazine) as a color additive. The usual dosage should be checked in the accompanying literature. The package contains 500 tablets with the NDC number 82009-079-05. It should be stored in a tightly sealed container at a temperature between 20°C to 25°C (68°F to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F). The code number is MHDRUGS/AD/018. There is a warning to keep the tablets out of reach of children and they should not be split. The tablets are manufactured by Ajanta Pharma Limited in India and are manufactured for Quallent Pharmaceuticals Health LLC in Grand Cayman, Cayman Islands.*

Each film-coated tablet contains Tadalafi, USP 5 mg. This medication is indicated for the treatment of erectile dysfunction in adult men. It should be taken orally with or without food, as directed by a healthcare professional. Tadalafil, the active ingredient in this medication, works by increasing blood flow to the penis, allowing for a firmer and longer-lasting erection. It is important to note that this medication should not be taken by individuals who are allergic to Tadalafil or any of the other ingredients in the tablet. Common side effects may include headache, flushing, upset stomach, and back pain. Please consult with a healthcare professional for more information.*