Oxybutynin Chloride

Product NDC

55154-6298

11-digit product format

551546298

Labeler code

55154

Product ID

55154-6298_0ecc3aa8-eb0e-45dc-b04e-44e68faddd4e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Cardinal Health

Application

ANDA076644

Marketing category

ANDA

Marketing start

2013-05-20

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record