NDC 71335-1729 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC71335-1729

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin Succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210224
Marketed since
May 21, 2019
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
71335-1729-130 TABLET, FILM COATED in 1 BOTTLE (71335-1729-1)Sep 23, 2021
71335-1729-290 TABLET, FILM COATED in 1 BOTTLE (71335-1729-2)May 30, 2024

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