Oxybutynin Chloride

Product NDC

68788-6402

11-digit product format

687886402

Labeler code

68788

Product ID

68788-6402_3d3647fb-4b84-4a36-9e90-cb34c41aa314

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA075079

Marketing category

ANDA

Marketing start

2016-06-09

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

2020-12-31

Current FDA listing

Historical FDA.report record