Solifenacin Succinate

Product NDC

51991-894

11-digit product format

519910894

Labeler code

51991

Product ID

51991-894_10b5e0ba-f68b-45f8-b09c-c79de33480bc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Solifenacin Succinate

Dosage form

TABLET

Route

ORAL

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA209818

Marketing category

ANDA

Marketing start

2019-05-20

Marketing end

0000-00-00

Substance

SOLIFENACIN SUCCINATE

Active strength

10 mg/1

Pharmacologic classes

Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record