NDC 72303-0831 – Solifenacin succinate

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

Human Prescription Drug

Product NDC72303-0831

Product details

Brand name
Solifenacin succinate
Generic name
Solifenacin succinate
Labeler
HEC Pharm USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213346
Marketed since
July 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72303-0831-130 TABLET, FILM COATED in 1 BOTTLE (72303-0831-1)Jul 1, 2026
72303-0831-290 TABLET, FILM COATED in 1 BOTTLE (72303-0831-2)Jul 1, 2026

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