Oxybutynin Chloride

Product NDC

51079-722

11-digit product format

510790722

Labeler code

51079

Product ID

51079-722_7d631f39-52c5-1814-e053-2991aa0a92ed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076702

Marketing category

ANDA

Marketing start

2006-11-27

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

5 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