OXYTROL

Product NDC

52544-920

11-digit product format

525440920

Labeler code

52544

Product ID

52544-920_f59c07ba-71fe-4a49-aa7e-f34b077df010

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxybutynin

Dosage form

PATCH

Route

TRANSDERMAL

Labeler

Actavis Pharma, Inc.

Application

NDA021351

Marketing category

NDA

Marketing start

2003-02-26

Marketing end

2020-01-31

Substance

OXYBUTYNIN

Active strength

4 mg/d

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record