NDC 68382-480 – Fesoterodine fumarate

Fesoterodine Fumarate 8 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68382-480

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

Uses, dosage, side effects and warnings for Fesoterodine Fumarate →

Package NDC codes (3)

Package NDCDescriptionSince
68382-480-0630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-06)Dec 7, 2017
68382-480-1690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-16)Dec 7, 2017
68382-480-7710 BLISTER PACK in 1 CARTON (68382-480-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-480-30)Dec 7, 2017

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