NDC 67877-528 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC67877-528

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin Succinate
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210224
Marketed since
May 21, 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
67877-528-3030 TABLET, FILM COATED in 1 BOTTLE (67877-528-30)May 21, 2019
67877-528-3810 BLISTER PACK in 1 CARTON (67877-528-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-528-33)May 21, 2019
67877-528-9090 TABLET, FILM COATED in 1 BOTTLE (67877-528-90)May 21, 2019

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