NDC 71205-583 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC71205-583

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin Succinate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209333
Marketed since
May 20, 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 (3)

Package NDCDescriptionSince
71205-583-3030 TABLET, FILM COATED in 1 BOTTLE (71205-583-30)Jun 25, 2021
71205-583-6060 TABLET, FILM COATED in 1 BOTTLE (71205-583-60)Jun 25, 2021
71205-583-9090 TABLET, FILM COATED in 1 BOTTLE (71205-583-90)Jun 25, 2021

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