NDC 0591-3795 – Solifenacin succinate

Solifenacin Succinate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0591-3795

Product details

Brand name
Solifenacin succinate
Generic name
Solifenacin succinate
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202551
Marketed since
June 30, 2020
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Solifenacin Succinate →

Package NDC codes (2)

Package NDCDescriptionSince
0591-3795-1990 TABLET, FILM COATED in 1 BOTTLE (0591-3795-19)Jun 30, 2020
0591-3795-3030 TABLET, FILM COATED in 1 BOTTLE (0591-3795-30)Jan 23, 2023

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