NDC 82804-058 – Solifenacin succinate

Solifenacin Succinate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82804-058

Product details

Brand name
Solifenacin succinate
Generic name
Solifenacin succinate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202551
Marketed since
April 9, 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 (3)

Package NDCDescriptionSince
82804-058-3030 TABLET, FILM COATED in 1 BOTTLE (82804-058-30)Jan 15, 2024
82804-058-6060 TABLET, FILM COATED in 1 BOTTLE (82804-058-60)Jan 15, 2024
82804-058-9090 TABLET, FILM COATED in 1 BOTTLE (82804-058-90)Jan 15, 2024

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