Oxybutynin Chloride

Product NDC

70518-0202

11-digit product format

705180202

Labeler code

70518

Product ID

70518-0202_99f48658-b9cb-253e-e053-2a95a90a20d4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxybutynin Chloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074625

Marketing category

ANDA

Marketing start

2017-02-06

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