NDC 31722-028 – Solifenacin succinate

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

Human Prescription Drug

Product NDC31722-028

Product details

Brand name
Solifenacin succinate
Generic name
Solifenacin succinate
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215761
Marketed since
June 15, 2022
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
31722-028-3030 TABLET, FILM COATED in 1 BOTTLE (31722-028-30)Jun 15, 2022
31722-028-3110 BLISTER PACK in 1 CARTON (31722-028-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-028-32)Jun 15, 2022
31722-028-9090 TABLET, FILM COATED in 1 BOTTLE (31722-028-90)Jun 15, 2022

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