NDC 35561-286 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC35561-286

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin succinate
Labeler
Bostal LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210281
Marketed since
May 20, 2019
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
35561-286-00129032 TABLET, FILM COATED in 1 BOX (35561-286-00)May 20, 2019
35561-286-1030 TABLET, FILM COATED in 1 BOTTLE (35561-286-10)May 20, 2019
35561-286-1190 TABLET, FILM COATED in 1 BOTTLE (35561-286-11)May 20, 2019
35561-286-13500 TABLET, FILM COATED in 1 BOTTLE (35561-286-13)May 20, 2019

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