GELNIQUE

Product NDC

0023-5812

11-digit product format

000235812

Labeler code

0023

Product ID

0023-5812_74ccc9f4-e4c5-472a-9087-39389aefda50

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

GEL

Route

TRANSDERMAL

Labeler

Allergan, Inc.

Application

NDA022204

Marketing category

NDA

Marketing start

2017-04-01

Marketing end

2020-10-31

Substance

OXYBUTYNIN CHLORIDE

Active strength

100 mg/g

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