NDC 68382-479 – Fesoterodine fumarate
Fesoterodine Fumarate 4 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68382-479
Product details
- Brand name
- Fesoterodine fumarate
- Generic name
- Fesoterodine fumarate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- 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 4 mg/1
Uses, dosage, side effects and warnings for Fesoterodine Fumarate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68382-479-06 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-06) | Dec 7, 2017 |
| 68382-479-16 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-16) | Dec 7, 2017 |
| 68382-479-77 | 10 BLISTER PACK in 1 CARTON (68382-479-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-479-30) | Dec 7, 2017 |
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