NDC 70771-1169 – Fesoterodine fumarate
Fesoterodine Fumarate 8 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70771-1169
Product details
- Brand name
- Fesoterodine fumarate
- Generic name
- Fesoterodine fumarate
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204946
- Marketed since
- December 7, 2017
- Listing expires
- December 31, 2026
Active ingredients
- Fesoterodine Fumarate 8 mg/1
Uses, dosage, side effects and warnings for Fesoterodine Fumarate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1169-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-3) | Dec 7, 2017 |
| 70771-1169-4 | 10 BLISTER PACK in 1 CARTON (70771-1169-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1169-2) | Dec 7, 2017 |
| 70771-1169-9 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-9) | Dec 7, 2017 |
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