NDC 65862-879 – Solifenacin Succinate

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

Human Prescription Drug

Product NDC65862-879

Product details

Brand name
Solifenacin Succinate
Generic name
Solifenacin Succinate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206817
Marketed since
December 27, 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 (4)

Package NDCDescriptionSince
65862-879-033 BLISTER PACK in 1 CARTON (65862-879-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-879-10)Dec 27, 2022
65862-879-3030 TABLET, FILM COATED in 1 BOTTLE (65862-879-30)Dec 27, 2022
65862-879-9090 TABLET, FILM COATED in 1 BOTTLE (65862-879-90)Dec 27, 2022
65862-879-991000 TABLET, FILM COATED in 1 BOTTLE (65862-879-99)Dec 27, 2022

Other Solifenacin Succinate products