Oxybutynin Chloride

Product NDC

50436-4777

11-digit product format

504364777

Labeler code

50436

Product ID

50436-4777_ddfe8060-bf75-44e2-80aa-39ea9d42705e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxybutynin Chloride

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA071655

Marketing category

ANDA

Marketing start

1990-09-30

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