NDC 31722-034 – Fesoterodine Fumarate

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

Human Prescription Drug

Product NDC31722-034

Product details

Brand name
Fesoterodine Fumarate
Generic name
Fesoterodine Fumarate
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204792
Marketed since
January 9, 2024
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
31722-034-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-30)Jan 9, 2024
31722-034-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-90)Jan 9, 2024

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