oxybutynin chloride

Product NDC

0615-7521

11-digit product format

006157521

Labeler code

0615

Product ID

0615-7521_e53fc330-b0d8-4441-8c1e-8562042d3bb4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

NDA020897

Marketing category

NDA

Marketing start

2007-05-10

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

15 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record