OXYBUTYNIN CHLORIDE

Product NDC

0093-5208

11-digit product format

000935208

Labeler code

0093

Product ID

0093-5208_b46c253f-c473-4b5f-a00b-cb775fae0c2c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

OXYBUTYNIN CHLORIDE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

TEVA Pharmaceuticals USA Inc

Application

ANDA076745

Marketing category

ANDA

Marketing start

2006-11-10

Marketing end

2020-08-31

Substance

OXYBUTYNIN CHLORIDE

Active strength

15 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