Vardenafil Hydrochloride 00093-7655
Product NDC
00093-7655- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 3, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA091347
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Vardenafil Hydrochloride | 20 mg/1 |
Drug Class
Phosphodiesterase 5 Inhibitor [EPC]Phosphodiesterase 5 Inhibitors [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (0093-7655-56)