NDC 67184-0517 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC67184-0517

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin Succinate Tablets
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209333
Marketed since
April 1, 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 (4)

Package NDCDescriptionSince
67184-0517-130 TABLET, FILM COATED in 1 BOTTLE (67184-0517-1)Apr 1, 2020
67184-0517-290 TABLET, FILM COATED in 1 BOTTLE (67184-0517-2)Apr 1, 2020
67184-0517-32000 TABLET, FILM COATED in 1 BOTTLE (67184-0517-3)Apr 1, 2020
67184-0517-440 TABLET, FILM COATED in 1 BLISTER PACK (67184-0517-4)Apr 1, 2020

Other Solifenacin Succinate products