oxybutynin chloride

Product NDC

55700-647

11-digit product format

557000647

Labeler code

55700

Product ID

55700-647_90649df5-c8f7-4304-8507-3ce4228b11ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA207138

Marketing category

ANDA

Marketing start

2018-07-06

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