NDC 70771-1168 – Fesoterodine fumarate

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

Human Prescription Drug

Product NDC70771-1168

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

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

Package NDC codes (3)

Package NDCDescriptionSince
70771-1168-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-3)Dec 7, 2017
70771-1168-410 BLISTER PACK in 1 CARTON (70771-1168-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1168-2)Dec 7, 2017
70771-1168-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-9)Dec 7, 2017

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