NDC 69238-1349-3
Tadalafil 20 mg/1
Tadalafil · TABLET, FILM COATED
Tadalafil is a phosphodiesterase 5 inhibitor tablet taken by mouth that is used to treat erectile dysfunction and symptoms of benign prostatic hyperplasia. It is available as a prescription medication in a 20 mg strength.
Key Facts
- Brand Name
- Tadalafil
- Generic Name
- Tadalafil
- NDC Code (Package)
69238-1349-3- NDC Code (Product)
69238-1349- Manufacturer
- Amneal Pharmaceuticals NY LLC
- Strength
- 20 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA209744
- Drug Class
- Phosphodiesterase 5 Inhibitor [EPC]
- Marketing Start
- 03/27/2019
Recall History
No Recall HistoryView Full Drug Page
Tadalafil — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.