Tadalafil 68180-0914
Product NDC
68180-0914- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 11, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA210572
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tadalafil | 20 mg/1 |
Drug Class
Phosphodiesterase 5 Inhibitor [EPC]Phosphodiesterase 5 Inhibitor [EPC]Phosphodiesterase 5 Inhibitors [MoA]