Tadalafil 68382-0899
Product NDC
68382-0899- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 27, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA206693
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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(6)
100 TABLET, FILM COATED in 1 BOTTLE (68382-899-01)
500 TABLET, FILM COATED in 1 BOTTLE (68382-899-05)
30 TABLET, FILM COATED in 1 BOTTLE (68382-899-06)
1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)
90 TABLET, FILM COATED in 1 BOTTLE (68382-899-16)
2 BLISTER PACK in 1 CARTON (68382-899-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK