Oxybutynin Chloride

Product NDC

55154-6647

11-digit product format

551546647

Labeler code

55154

Product ID

55154-6647_17392900-2a95-4e56-802d-eb60b4f254d9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health

Application

ANDA075079

Marketing category

ANDA

Marketing start

2010-01-13

Marketing end

2020-10-31

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

0000-00-00

Current FDA listing

Historical FDA.report record