Fesoterodine Fumarate 70771-1169
Product NDC
70771-1169- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 7, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204946
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fesoterodine Fumarate | 8 mg/1 |
Packaging Options(3)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-3)
10 BLISTER PACK in 1 CARTON (70771-1169-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1169-2)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-9)