OXYBUTYNIN CHLORIDE

Product NDC

63629-6355

11-digit product format

636296355

Labeler code

63629

Product ID

63629-6355_173f4419-9f97-4081-8547-8afdee5023b6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

OXYBUTYNIN CHLORIDE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076745

Marketing category

ANDA

Marketing start

2007-05-11

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