NDC 72603-413 – Fesoterodine Fumarate

Fesoterodine Fumarate 4 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC72603-413

Product details

Brand name
Fesoterodine Fumarate
Generic name
Fesoterodine Fumarate
Labeler
NorthStar RxLLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204792
Marketed since
May 1, 2024
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72603-413-0130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-413-01)May 1, 2024

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