Oxybutynin Chloride

Product NDC

51079-723

11-digit product format

510790723

Labeler code

51079

Product ID

51079-723_9af1ad6d-7933-2bba-e053-2a95a90a819a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076644

Marketing category

ANDA

Marketing start

2006-11-27

Marketing end

2020-01-31

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

0000-00-00

Current FDA listing

Historical FDA.report record