Tadalafil 68071-3777
Product NDC
68071-3777- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 26, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA209250
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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]
Packaging Options(3)
24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-4)
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-5)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-6)