Oxybutynin Chloride

Product NDC

70518-0965

11-digit product format

705180965

Labeler code

70518

Product ID

70518-0965_8f6ee50e-a961-24ba-e053-2995a90a68a2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076644

Marketing category

ANDA

Marketing start

2018-01-18

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

10 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